Ardent Intl., Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Advertisement
Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K864300 | SILIVA EJECTOR/ORAL CAVITY EVACUATOR | DYN | 1986-11-24 | View |
| 510(k) | K842512 | EXACTA-FILM | 1984-06-27 | View | |
| 510(k) | K832647 | ARTICULATING PAPER | EFH | 1984-02-21 | View |
No matching devices.
Advertisement