# Smec, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 7 (1980–1985): 7 510(k) clearances
- Product codes: DSP (7)
- 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
- K840367: Pressure Trigger Mod of Smec Intra-Aort (Dec 11, 1985)
- K840037: Modified Smec Percutaneous Intra-Aortic (Feb 1, 1985)
- K832753: Percutaneous Balloon (Oct 13, 1984)
- K823739: Intra-Aortic Balloon System (Feb 18, 1983)
- K823177: Smec Balloon System (Dec 15, 1982)
- K813355: Modification of the Percutan-Balloon (Jul 2, 1982)
- K790755: Smec Balloon Cannula (May 14, 1980)

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