# Zimmer Patient Care Division

- Location (FDA's records): Dover, OH
- FDA decisions: 3 (1993–1996): 3 510(k) clearances
- Product codes: FMQ (1), CAC (1), GCJ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)

## Its most-cited devices
- K920273: Hemovac Autotransfusion System (1993), cited by 1

## Recent decisions
- K963435: Economy Safety Vest Restraint, Shoulder Tie Safety Vest/Safety Vest Restraint, Heavy Duty Vest Restraint, Mesh Safety VE (Nov 6, 1996)
- K935709: General Surgery Probe/General Surgery Probe W/Distal Perforations (Jan 31, 1994)
- K920273: Hemovac Autotransfusion System (Jan 28, 1993)

Source page: https://510kreport.com/company/zimmer-patient-care-division