Company ยท US
Metrika, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2005. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 13, 2005 | K051321 | INVIEW Metrika, Inc. | LCP |
| Dec 23, 2003 | K033847 | A1CNOW FOR HOME AND PROFESSIONAL USE Metrika, Inc. | LCP |
| Dec 13, 2002 | K022661 | A1CNOW FOR HOME USE Metrika, Inc. | LCP |
| Feb 15, 2002 | K020235 | A1CNOW FOR PROFESSIONAL USE Metrika, Inc. | LCP |
| Feb 15, 2002 | K020234 | A1CNOW FOR RX HOME USE Metrika, Inc. | LCP |
| Sep 26, 2000 | K000885 | DRX HBA1C - FOR PRESCRIPTION HOME USE Metrika, Inc. | LCP |
| Jul 26, 2000 | K000887 | DRX HBA1C Metrika, Inc. | LCP |
| Nov 9, 1999 | K992997 | OSTEOMARK NTX POC Metrika, Inc. | JMM |
| Sep 17, 1999 | K991532 | DRX QT. HCG Metrika, Inc. | DHA |
| Aug 10, 1999 | K984530 | DRX NTX OR, OSTEOMARK NTX DIRECT RESPONSE Metrika, Inc. | JFY |
| Jul 12, 1999 | K991917 | OSTEOMARK NTX POINT OF CARE (POC) CONTROL SET Metrika, Inc. | JJW |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 31, 2007 | Metrika Inc A1CNOW+ with sampler 10-Test Kits (Product No: 3022), Metrika, Inc., Sunnyvale, CA 94085. (This test provides quantitative measurement of the percent of glycated hemoglobin (%A1C) levels in capillary Terminated |
LCP | K051321 |