Primus, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K993131 | NYCOCARD HBA1C GLYCOSYLATED HEMOGLOBIN ASSAY | LCP | 2000-05-22 | View |
| 510(k) | K896582 | DIABETES CARE(TM) TEST PACKAGE FOR THE CLC 330(TM) | LCP | 1990-06-28 | View |
| 510(k) | K891235 | PRIMUS MODEL CLC 330 | LCP | 1989-06-16 | View |
No matching devices.
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