# Aeroquip Medical Products

- Location (FDA's records): Ann Arbor, MI
- FDA decisions: 2 (1997–1997): 2 510(k) clearances
- Product codes: FOZ (2)
- 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
- K970669: Aeroquip Safestart IV Catheter (Aug 1, 1997)
- K970644: Aeroquip Safestart (TM) IV Cath (TM) System (Jul 31, 1997)

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