# Mckinley Infuser

- Location (FDA's records): San Francisco, CA
- FDA decisions: 1 (2002–2002): 1 510(k) clearance
- Product codes: MEB (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Breg, Inc.: 1 (https://510kreport.com/company/breg)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- I-Flow Corp.: 1 (https://510kreport.com/company/i-flow)

## Firms that cite its devices most
- Mckinley, Inc.: 2 (https://510kreport.com/company/mckinley)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)

## Its most-cited devices
- K023098: Accufuser, Accufuser Plus, Standard Procedure Kit, Accufuser Infusion Kit (2002), cited by 3

## Recent decisions
- K023098: Accufuser, Accufuser Plus, Standard Procedure Kit, Accufuser Infusion Kit (Dec 9, 2002)

Source page: https://510kreport.com/company/mckinley-infuser