# American Mcgaw

- Location (FDA's records): Mchenry, IL
- FDA decisions: 13 (1981–1985): 13 510(k) clearances
- Product codes: FPA (3), KPE (2), FKX (2), LHI (1), FLN (1), FDA (1), KFX (1), KDJ (1), FRN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 8 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Mcgaw, Inc.: 2 (https://510kreport.com/company/mcgaw)

## Its most-cited devices
- K840212: Concentrated Platelet Admin. Set (1984), cited by 1
- K820133: Mcgaw Fat Emulsion Set (1982), cited by 1

## Recent decisions
- K853549: Mcgaw/Drop Watch Flow Monitor (Nov 12, 1985)
- K843639: Add-a-Vial Solution Transfer Device (Jan 14, 1985)
- K843954: Mixing Container (Nov 28, 1984)
- K841729: Accupro Enteral Feeding Pump (Jun 1, 1984)
- K840388: Pab  IV Container (Mar 6, 1984)
- K840212: Concentrated Platelet Admin. Set (Mar 6, 1984)
- K831716: Capd - Catheter Adapter (Jun 24, 1983)
- K822240: Ethylene Oxide Steriliz. Parametric Rel. (Dec 30, 1982)

Source page: https://510kreport.com/company/american-mcgaw