# Windsor Medical, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1983–1984): 9 510(k) clearances
- Product codes: FRN (8), FRW (1)
- 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
- K841481: Windsor Medical Model 50-00002 (May 21, 1984)
- K832606: Windsor Medical Various Models (Nov 29, 1983)
- K832641: Windsor Medical Model 52 (Oct 4, 1983)
- K830657: Ambulatory Mark XI Drug Infusion Dev- (Sep 16, 1983)
- K830656: Ambulatory Mark Iii Infusion Device (Aug 16, 1983)
- K830317: Infusion Pump Access. #60-01-5 (Mar 31, 1983)
- K830544: Windsor Medical, Inc. 50-01-028 (Mar 31, 1983)
- K830490: MODEL 50-01-27 (Mar 31, 1983)

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