Home › e-Linkcare Meditech Co., Ltd › Uric Acid Control solution(level 2)
Uric Acid Control solution(level 2)
e-Linkcare Meditech Co., Ltd · Model CM311 · UDI-DI 06971404131628
5
510(k) clearances
1
Adverse events
1
Recalls
3
Facilities
Description
It is used to confirm that your Blood Uric Acid Test Strips and Multi-Monitoring Meter are working together properly and that you are performing the test correctly.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-07-20 | Sterling Diagnostics, Inc. | Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple diagnostic kits due to a recision of the previously extended expiration dates for the kits. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.