Vitatek
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K823052 | THE 500 MONITOR SERIES | DXN | 1982-11-30 | View |
| 510(k) | K810755 | SQUINN VITATEK 500 SERIES PHYSIOL. MONI | DRT | 1981-04-03 | View |
No matching devices.
Advertisement