# Avco Medical Products

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1977–1981): 5 510(k) clearances
- Product codes: DSP (4), KFM (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
- K802924: Kontron Percutaeous Double-Lumen (Mar 11, 1981)
- K790241: Intra-Aortic Balloon-Pump (Feb 23, 1979)
- K781848: Pump, Balloon Model 10 (Jan 23, 1979)
- K770937: Pump, Bypass, Pulsatile, Avco (Nov 17, 1977)
- K770821: Pump, Balloon, Intra-Aortic, Tri-Segment (May 6, 1977)

Source page: https://510kreport.com/company/avco-medical-products