Control™ Meter Kit

Catalogue number IGM-0009, listed by U. S. Diagnostics, Inc., United States, under Glucose Oxidase, Glucose. 8 manufacturers in China are registered for this product code.

Registry build 21.09.26
8manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (3), Zhejiang (2), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CGA
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
Flextronics Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Yasee Biomedical Inc Qingdao Shandong Contract manufacturer 5
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Vivachek Biotech (Hangzhou) Co., Ltd. Hangzhou, Zhuji Zhejiang Contract manufacturer 21
Shenzhen Yuwen E-Commerce Co., Ltd. Shenzhen Guangdong Repacker / relabeller 19
Tianjin Empecs Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 8

Record

Regulatory record for Control™ Meter Kit
Listed by U. S. Diagnostics, Inc., United States
FDA product code CGA
Device type Glucose Oxidase, Glucose
Device class Class 2
Regulation 21 CFR 862.1345
Record published 2017-10-26
Record revised 2024-11-11 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Over the counter Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Handling environment temperature 50 to 104 °F; Handling environment humidity 10 to 90 % RH
Sizes Total volume 1 Microliter

Catalogue Numbers

Catalogue numbers for Control™ Meter Kit
Catalogue number Size Status
IGM-0009 Total Volume 1 Microliter In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
i-STAT Abbott Point OF Care Inc. 48
YSI Incorporated YSI Incorporated 34
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 28
Stat Profile Nova Biomedical Corporation 17
Fora Fora Care Inc. 13
TRUEtrack Trividia Health, Inc. 12
JAS Diagnostics Drew Scientific, Ltd. 11
StatStrip Nova Biomedical Corporation 9
Gluc-PAP Randox Laboratories Limited 8
Nova Primary Nova Biomedical Corporation 8
Synermed® Infrared Laboratory Systems LLC 7
Prodigy No Coding Blood Glucose Test Strips Prodigy Diabetes Care, LLC 7

Showing 12 of 215. All products under Glucose Oxidase, Glucose

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K061431 2007-01-12
K862721 1986-09-03

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P990026 2002-02-04 CYGNUS GLUCOWATCH AUTOMATIC GLUCOSE BIOGRAPHER Animas Corp.

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