Thomas J. Fogarty, M.D.
FDA 510(k) & PMA Approved Devices — 6 products
Advertisement
Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K902453 | OSCILLOMETRIC PULSE DETECTION DEVICE | DRS | 1990-08-23 | View |
| 510(k) | K884154 | TRANSLUMINAL ENDARTERECTOMY DEVICE | LIF | 1988-12-27 | View |
| 510(k) | K831809 | FOGARTY OCCLUDER PAD | DXC | 1984-08-27 | View |
| 510(k) | K841310 | GASTROINTESTINAL DILATOR | KNQ | 1984-07-31 | View |
| 510(k) | K834451 | COAXIAL BALLOON GASTROESOPHAGEAL DILA | KNQ | 1984-02-04 | View |
| 510(k) | K831384 | COAXIAL BALLOON URETHRAL DILATOR | FAH | 1983-07-26 | View |
No matching devices.
Advertisement