Boehringer Mannheim Italia Spa
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) | K955266 | ACCUSTAT HCG SERUM DILUENT REAGENT OR EVENT SERUM DILUENT | JHI | 1996-02-29 | View |
| 510(k) | K936013 | EVATEST STRIP | LCX | 1994-02-25 | View |
| 510(k) | K935502 | EVENT TEST STRIP HCG | JHI | 1994-01-27 | View |
No matching devices.
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