ReliOn™ Fast A1C Test

The ReliOn™ Fast A1C Test provides quantitative measurement of the percent of glycated hemoglobin (%HbA1C or %A1C) levels in human whole blood samples.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number

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 ReliOn™ Fast A1C Test
Listed by Wal Mart Stores, Inc
FDA product code LCP
Device type Assay, Glycosylated Hemoglobin
Device class Class 2
Regulation 21 CFR 864.7470
510(k) K090413
Record published 2016-09-01
Record revised 2021-10-14 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Over the counter Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Special storage condition: Avoid running test on hot or cold surfaces or near sources of hot or cold.; Special storage condition: If test has recently been at temperatures above 77 degrees F / 25 C, or below 64 F / 18 C, allow all kit parts to come t; Special storage condition: If you cannot store the kit under these recommended conditions, you may refrigerate the kit (do not freeze). However you; Special storage condition: Use at room temperature (64-77 degrees F / 18-25 C) and out of direct sunlight.; Special storage condition: Do not use if seal is missing or broken. Do not use if dot is red or if the product is past the expiration date.; Storage environment temperature 64 to 77 °F
Distribution end date 2018-03-27

Catalogue Numbers

Catalogue numbers for ReliOn™ Fast A1C Test
Catalogue number Size Per pack Status
3055 2 Withdrawn

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
Drew Scientific Drew Scientific, Ltd. 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

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

Recalls Naming This Product

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

Recalls naming the identifiers of ReliOn™ Fast A1C Test
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Polymer Technology Systems 510(k) number 2024-09-18 Class II Under Investigation by firm The reason for this recall is PTS Diagnostics, Inc. received complaints of non-matching cartridge and analyzer codes within the product test system box. Use of cartridges and analyzers with non-matching codes may result in inaccurate test r 2,452 units
Polymer Technology Systems 510(k) number 2016-12-02 Class II Software design A numerical value less than 4% or greater than 13% may be displayed instead of the expected <4% or >13% result, due to a software bug. 112,648 2020-07-16
Polymer Technology Systems 510(k) number 2016-12-02 Class II Software design A numerical value less than 4% or greater than 13% may be displayed instead of the expected <4% or >13% result, due to a software bug. 500 2020-07-16
Polymer Technology Systems 510(k) number 2016-12-02 Class II Software design A numerical value less than 4% or greater than 13% may be displayed instead of the expected <4% or >13% result, due to a software bug. 15,118 2020-07-16
Polymer Technology Systems 510(k) number 2016-12-02 Class II Software design A numerical value less than 4% or greater than 13% may be displayed instead of the expected <4% or >13% result, due to a software bug. 20,825 2020-07-16
Polymer Technology Systems 510(k) number 2016-12-02 Class II Software design A numerical value less than 4% or greater than 13% may be displayed instead of the expected <4% or >13% result, due to a software bug. 8285 2020-07-16
Bayer Healthcare LLC, Consumer Care 510(k) number 2013-08-26 Class II Nonconforming Material/Component Test results from these lots may produce a high-bias reading (by up to 20%) that is outside of limits defined for stability and product accuracy when product is stored at room temperature four (4) to five (5) months after release. 138 Kits in US (Total 2452) 2014-01-14

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