Metrika, Inc.
FDA 510(k) & PMA Approved Devices — 11 products
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Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K051321 | INVIEW | LCP | 2005-06-13 | View |
| 510(k) | K033847 | A1CNOW FOR HOME AND PROFESSIONAL USE | LCP | 2003-12-23 | View |
| 510(k) | K022661 | A1CNOW FOR HOME USE | LCP | 2002-12-13 | View |
| 510(k) | K020234 | A1CNOW FOR RX HOME USE | LCP | 2002-02-15 | View |
| 510(k) | K020235 | A1CNOW FOR PROFESSIONAL USE | LCP | 2002-02-15 | View |
| 510(k) | K000885 | DRX HBA1C - FOR PRESCRIPTION HOME USE | LCP | 2000-09-26 | View |
| 510(k) | K000887 | DRX HBA1C | LCP | 2000-07-26 | View |
| 510(k) | K992997 | OSTEOMARK NTX POC | JMM | 1999-11-09 | View |
| 510(k) | K991532 | DRX QT. HCG | DHA | 1999-09-17 | View |
| 510(k) | K984530 | DRX NTX OR, OSTEOMARK NTX DIRECT RESPONSE | JFY | 1999-08-10 | View |
| 510(k) | K991917 | OSTEOMARK NTX POINT OF CARE (POC) CONTROL SET | JJW | 1999-07-12 | View |
No matching devices.
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