# Smith

- Location (FDA's records): Crofton, MD
- FDA decisions: 5 (1997–1998): 5 510(k) clearances
- Product codes: EWO (1), FMQ (1), GEI (1), LGZ (1), LDQ (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
- K973747: Controlled Temperature Cabinet System (May 7, 1998)
- K973748: Tempo and Temp H20 (Mar 10, 1998)
- K972123: Protective Restraint Models #302,440,750,850,AND905 (Jul 25, 1997)
- K971092: QA-ES (Apr 23, 1997)
- K970555: IL0292 DP Echoport (Mar 17, 1997)

Source page: https://510kreport.com/company/smith