Thomas J. Fogarty, M.D.
Thomas J. Fogarty, M.D. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 23, 1990.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K902453 | OSCILLOMETRIC PULSE DETECTION DEVICE | August 23, 1990 |
| K884154 | TRANSLUMINAL ENDARTERECTOMY DEVICE | December 27, 1988 |
| K831809 | FOGARTY OCCLUDER PAD | August 27, 1984 |
| K841310 | GASTROINTESTINAL DILATOR | July 31, 1984 |
| K834451 | COAXIAL BALLOON GASTROESOPHAGEAL DILA | February 4, 1984 |
| K831384 | COAXIAL BALLOON URETHRAL DILATOR | July 26, 1983 |