Apogee, 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) | K992137 | UROLOGICAL CATHETER | GBM | 1999-09-03 | View |
| 510(k) | K942381 | LOW PRESSURE INJECTION TUBING, COILED LINE, EXTENSION TUBING | DXT | 1995-03-17 | View |
No matching devices.
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