Bionike, Inc.
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) | K990280 | BIONIKE AQ BARBITURATE TEST | DIS | 1999-06-28 | View |
| 510(k) | K970008 | ADVANCED QUALITY PREGNANCY TEST | LCX | 1997-02-18 | View |
No matching devices.
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