SoftTrack

61 catalogue numbers from 4.1.17.249, listed by SCC Soft Computer, United States, under Calculator/Data Processing Module, For Clinical Use. 7 manufacturers in China are registered for this product code.

Registry build 21.09.26
7manufacturers in China registered for this device type
61catalogue numbers in this listing
19recalls on this code

Who Else Makes It

Concentrated in Zhejiang (2), Guangdong (2), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JQP
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Zhejiang Gene Science Co., Ltd. Shaoxing Zhejiang Manufacturer 31
Foshan Zike Technology Co., Ltd. Foshan Guangdong Manufacturer 9
Tianjin Empecs Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 8
Shanghai Bestcovered Limited Shanghai Shanghai Manufacturer 2

Record

Regulatory record for SoftTrack
Listed by SCC Soft Computer, United States
FDA product code JQP
Device type Calculator/Data Processing Module, For Clinical Use
Device class Class 1
Regulation 21 CFR 862.2100
Establishment Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2024-12-21

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for SoftTrack
Catalogue number Size Status
4.1.17.249 In distribution
4.1.17.240 In distribution
4.2.0.7 In distribution
4.1.11.22 In distribution
4.1.17.239 In distribution
4.1.17.247 In distribution
4.1.17.5 In distribution
4.2.0.20 In distribution
3.4.3.27 In distribution
4.1.14.5 In distribution
4.1.17.242 In distribution
4.2.0.15 In distribution
4.1.17.30 In distribution
4.2.0.18 In distribution
4.1.17.232 In distribution
4.1.17.255 In distribution
4.2.0.24 In distribution
4.1.17.250 In distribution
3.4.3.26 In distribution
4.1.17.10 In distribution
4.1.17.20 In distribution
4.1.17.4 In distribution
4.1.17.244 In distribution
4.2.0.19 In distribution
4.1.11.17 In distribution
4.1.17.7 In distribution
4.3.0.0 In distribution
4.1.17.237 In distribution
4.2.0.21 In distribution
4.1.17.14 In distribution
4.1.17.252 In distribution
4.1.17.238 In distribution
4.3.0.3 In distribution
4.1.17.230 In distribution
4.1.17.236 In distribution
4.1.17.235 In distribution
4.1.17.234 In distribution
4.2.0.17 In distribution
4.1.15.6 In distribution
4.1.11.21 In distribution
4.1.17.246 In distribution
4.2.0.10 In distribution
4.1.11.16 In distribution
3.5.68.1 In distribution
4.1.17.23 In distribution
4.1.17.243 In distribution
4.1.18.0 In distribution
4.2.0.22 In distribution
4.1.17.248 In distribution
4.1.17.12 In distribution
4.1.17.251 In distribution
4.1.17.245 In distribution
4.1.17.233 In distribution
4.1.17.17 In distribution
4.1.17.241 In distribution
4.2.0.13 In distribution
4.1.17.254 In distribution
4.3.0.2 In distribution
4.3.0.1 In distribution
4.1.14.4 In distribution
4.1.17.253 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SoftPathDx SCC Soft Computer 69
SoftMolecular SCC Soft Computer 67
SoftFlowCytometry SCC Soft Computer 67
SoftBiochemistry SCC Soft Computer 67
SoftCytogenetics SCC Soft Computer 67
SoftMic SCC Soft Computer 65
SoftLab SCC Soft Computer 64
SoftHLA SCC Soft Computer 61
SoftGenomics SCC Soft Computer 51
SoftGenePortal SCC Soft Computer 48
SoftTotalQC SCC Soft Computer 28
Rals Abbott Rapid Diagnostics Informatics, Inc. 14

Showing 12 of 140. All products under Calculator/Data Processing Module, For Clinical Use

Recalls

6 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2021-03-31 Class II Software design (manufacturing process) Software is given wrong results going out to HIS on test that had reruns. 5 2023-02-14
2021-03-31 Class II Software Design Change Software showing wrong results reported, PDF not match HIS. 1 2022-04-15
2014-11-26 Class II Software design Modifications to diagnostic text may be: 1) Saved to the database but not appear on the report sent to the physician; or 2) Documented on the report, but not saved to the database. 108 units 2016-05-16
2014-05-20 Class II Device Design The interface fails to send abnormal flags for Reference Lab test results. 48 2016-05-16
2014-01-29 Class II Software design When an isolate is resulted without a SNOMED code, isolate information in the downstream system may be incomplete or missing. As a result, there is the potential for the delay or omission of patient treatment updates. 1 2014-11-03
2011-10-17 Class II Software design On 10/17/2011 SCC Soft Computer, Clearwater, FL initiated a correction on SoftLab with SA INST versions: 3.1.6.12, 4.0.1.26-4.0.1.32, 4.0.2.21-4.0.2.51, and 4.0.3.5-4.0.3.13. A client reported an issue which caused two different sets of res 88 2014-09-03
2011-08-25 Not classified Software design On 08/25/2011, SCC Soft Computer initiated a correction on the following SoftMic GUI versions: 4.0.3.0-4.0.3.15, 4.0.4.1-4.0.4.7. For clients using SoftMic Result Entry, when a certain series of keystrokes on the test grid are performed whi 144 2014-10-03
2011-08-08 Not classified Software design On 08/08/2011 SCC Soft Computer, Clearwater, FL initiated a correction on following SoftLab used with: SA BASE 3.1.4.x, 3.1.6.x and SA LabMic 4.0.0.x, 4.0.1.x, 4.0.2.x, 4.0.3.x, 4.0.4.x. A client reported a flagging error where the result 255 2013-11-22
2011-07-26 Not classified Software design SCC Soft Computer, Clearwater, FL, initiated a correction for the SoftLab used with SA INST. A test performed on the Roche Cobas Integra series of instruments when used with the GenInst/Dispatch listening program could cause incorrect flagg 265 2013-05-21
2011-07-20 Not classified Software design On 07/20/2011 SCC Soft Computer, Clearwater, FL, initiated a correction on the following SoftPath GUI versions: 4.2.3.3-4.2.3.6 and 4.3.0.5-4.3.0.12. A client reported that the HPV results on a patient report were incorrect. The HPV results 97 2013-05-21
2011-07-13 Not classified Software design Soft Computer, Clearwater, FL, initiated a correction on the following SoftPath GUI versions: 3.17.5 to 3.17.9, 4.2.1 to 4.2.3, and 4.3.0 to 4.3.0.4. SoftPath architecture does not correctly handle AP macros and data fields inside report se 142 2012-07-17
2011-05-03 Not classified Software design On 05/03/2011, SCC Soft Computer, Clearwater, FL, initiated a correction on the following SoftLab GUI versions: 3.18.1.0-3.18.1.21; 3.19.1.0-3.19.1.25; 3.19.2.0-3.19.2.21; 4.0.0.2; 4.0.1.0-4.0.1.16; 4.0.2.0-4.0.2.10; 4.0.3.0-4.0.3.16; 4.0.4 220 2013-08-07
2010-06-01 Not classified Software design Functionality issue: For clients using the instrument to generate results on the interface menu, two different result records could be displayed under the same order and sequence numbers. This could cause incorrect results to be populated 40 2012-07-16
2010-02-16 Not classified Software design When a test is being verified, the wrong (expired) ranges may be associated to that test result, causing an incorrect flag to be posted for that test result. 31 2012-07-17
2009-04-01 Not classified Software design Clients using Patient Maintenance to perform Moves of Stays may send the wrong billing number during an ADT update to SoftWeb, SoftPath or SoftMedia. The wrong billing number can come from a different patient in Order Entry. Only Moves of 49 2013-08-07
2006-02-23 Not classified Other Loss of text misrepresented individual tissue diagnosis on the final diagnosis print out from the HIS system software. The specimen heading “J” was removed and the diagnosis appeared under the specimen heading “I” as a result the specimen 335 2008-11-20
2006-02-23 Not classified Software design In the creation of revised report and supplemental reports diagnosis, text was inserted from another case. 201 2008-11-20
2004-10-27 Not classified Other Text from one case is overwriting another. This could cause an incorrect diagnostic report to be sent to a clinician/surgeon. 4 2010-07-19
2001-01-09 Not classified Other The client had made a decision to use the SoftPath Module in a nonstandard manner. Under specific circumstances, incorrect text may appear on a patient report. 171 2010-07-19

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer