# Thomas J. Fogarty, M.D.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1983–1990): 6 510(k) clearances
- Product codes: KNQ (2), DRS (1), FAH (1), LIF (1), DXC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K902453: Oscillometric Pulse Detection Device (Aug 23, 1990)
- K884154: Transluminal Endarterectomy Device (Dec 27, 1988)
- K831809: Fogarty Occluder Pad (Aug 27, 1984)
- K841310: Gastrointestinal Dilator (Jul 31, 1984)
- K834451: Coaxial Balloon Gastroesophageal Dila (Feb 4, 1984)
- K831384: Coaxial Balloon Urethral Dilator (Jul 26, 1983)

Source page: https://510kreport.com/company/thomas-j-fogarty-md