Bayer Group Diagnostics
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K020210 | GLUCOMETER DEX BLOOD GLUCOSE SYSTEM (MODIFIED) | NBW | 2002-04-30 | View |
| 510(k) | K020208 | GLUCOMETER ELITE DIABETES CARE SYSTEM (MODIFIED) | NBW | 2002-04-29 | View |
No matching devices.
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