Accutest iFOBT – Specimen Collection Tubes

Accutest iFOBT - Specimen collection tubes Contains: 25 Specimen collection tubes

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Zhejiang (2), Guangdong (1), Beijing (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 KHE
Manufacturer City Province Registered as Device types
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Hangzhou Genesis Biodetection & Biocontrol Co., Ltd. Hangzhou Zhejiang Contract manufacturer 5
Guangzhou Wondfo Biotech Co., Ltd. Guangzhou Guangdong Contract manufacturer 44
W.h.p.m. Bioresearch & Technology Co., Ltd. Beijing Beijing Manufacturer 37
Chong Qing Teco Huayi Pharm. Co. Shapingba Dist. Chongqing Contract manufacturer 18

Record

Regulatory record for Accutest iFOBT – Specimen Collection Tubes
Listed by Jant Pharmacal Corp., United States
FDA product code KHE
Device type Reagent, Occult Blood
Device class Class 2
Regulation 21 CFR 864.6550
Establishment Complaint-file establishment
510(k) K063693
Record published 2016-09-23
Record revised 2022-06-10 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Accutest iFOBT – Specimen Collection Tubes
Catalogue number Size Per pack Status
CS630 25 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OC-Light S Polymedco Cancer Diagnostic Products LLC 59
McKesson Mckesson Medical-Surgical Inc. 21
Hemosure Hemosure Inc. 21
Hemoccult Beckman Coulter, Inc. 17
Henry Schein Henry Schein, Inc. 14
PremierPro Prestige Ameritech 11
hema-screen Specific Immunostics, Inc. 9
InSure® ONE™ Enterix Inc. 8
InSure FIT Enterix Inc. 7
hema-screen Immunostics, Inc. 7
ADS Medical W.h.p.m., Inc. 7
QuickVue Quidel Corp. 6

Showing 12 of 135. All products under Reagent, Occult Blood

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Accutest iFOBT – Specimen Collection Tubes
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Alere North Americal 510(k) number 2011-03-21 Not classified Other Potential for false negatives test results and negative/faint positive controls 3900 kits 2013-03-07
Alere North Americal 510(k) number 2011-03-21 Not classified Other Potential for false negatives test results and negative/faint positive controls 1594 kits 2013-03-07
Alere North Americal 510(k) number 2011-03-21 Not classified Other Potential for false negatives test results and negative/faint positive controls 1800 units 2013-03-07
Alere North Americal 510(k) number 2011-03-21 Not classified Other Potential for false negatives test results and negative/faint positive controls 500 units 2013-03-07

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