# Houston Biomedical, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 3 (1986–1987): 3 510(k) clearances
- Product codes: FGE (1), KOD (1), DQO (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
- K861291: Gastrotopo (May 15, 1987)
- K861241: Angiotopo Catheter (Jan 6, 1987)
- K861200: Urotopo Catheter (Apr 23, 1986)

Source page: https://510kreport.com/company/houston-biomedical