Bio-Rad Laboratories, Inc., Clinical Systems Divis
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) | K130990 | VARIANT(TM) II TURBO HBA1C KIT - 2.0 | LCP | 2013-05-09 | View |
| 510(k) | K130860 | VARIANT II HEMOGLOBIN A1C PROGRAM (NEW), VARIANT II HEMOGLOBIN TESTING SYSTEM WITH CDM SOFTWARE, CDM SOFTWARE | LCP | 2013-04-25 | View |
| 510(k) | K122472 | VARIANT II TURBO HBA1C KIT-2.0 VARIANT II TURBO HEMOGLOBIN TESTING SYSTEM | LCP | 2012-10-26 | View |
No matching devices.
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