# Mckinley Medical, LLC

- Location (FDA's records): Wheat Ridge, CO
- FDA decisions: 2 (2005–2006): 2 510(k) clearances
- Product codes: FRN (1), MEB (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 2 (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
- Micor, Inc.: 2 (https://510kreport.com/company/micor)
- I-Flow Corp.: 2 (https://510kreport.com/company/i-flow)
- Mckinley, Inc.: 1 (https://510kreport.com/company/mckinley)

## Firms that cite its devices most
- Westmed, Inc.: 1 (https://510kreport.com/company/westmed)
- Mps Acacia: 1 (https://510kreport.com/company/mps-acacia)

## Its most-cited devices
- K050770: Modification to Accufuser, Accufuser Plus Standard Procedure Kit (2005), cited by 2

## Recent decisions
- K060119: Mckinley Saturation Catheter (Apr 12, 2006)
- K050770: Modification to Accufuser, Accufuser Plus Standard Procedure Kit (Apr 14, 2005)

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