Drew Scientific

DS360 HbA1c Analyzer with accessories

Registry build 21.09.26
3manufacturers in China registered for this device type
5catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (1).

Chinese manufacturers registered for FDA product code LCP
Manufacturer City Province Registered as Device types
Wuxi Biohermes BIO & Medical Technology Co., Ltd. Wuxi Jiangsu Manufacturer 3
Shanghai Medconn Medical Technology Co., Ltd. Shanghai Shanghai Manufacturer 2
Shanghai Medconn Biotechnology Co., Ltd. Jinshan District Shanghai Manufacturer 2

Record

Regulatory record for Drew Scientific
Listed by Drew Scientific, Ltd., United Kingdom
FDA product code LCP
Device type Assay, Glycosylated Hemoglobin
Device class Class 2
Regulation 21 CFR 864.7470
510(k) K933287
Record published 2016-09-09
Record revised 2023-08-03 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 18 to 30 °C

Catalogue Numbers

Catalogue numbers for Drew Scientific
Catalogue number Size Status
DSJ-9001-001 In distribution
014-081 In distribution
014-350 In distribution
099-023 In distribution
014-080 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Trinity Biotech Primus Corp. 36
Variant II Turbo Bio-Rad Laboratories Inc. 15
Pointe Scientific, Inc. Horiba Instruments Incorporated 11
Variant II Turbo Link Bio-Rad Laboratories Inc. 7
D-10 Bio-Rad Laboratories Inc. 7
Variant II Hemoglobin A1c Bio-Rad Laboratories Inc. 5
Tosoh Automated Glycohemoglobin Analyzer HLC-723GR01 Tosoh Corp. 4
D-100 Bio-Rad Laboratories Inc. 4
Fructosamine Roche Diagnostics Gmbh 4
D-10 Dual Bio-Rad Laboratories Inc. 3
JAS Diagnostics Drew Scientific, Ltd. 3
Henry Schein Henry Schein, Inc. 2

Showing 12 of 134. All products under Assay, Glycosylated Hemoglobin

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K933287 1993-09-09
K920198 1992-07-21

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