# Phoenix Glove Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1978–1983): 6 510(k) clearances
- Product codes: FMC (2), FRG (1), DRX (1), FJZ (1), KKX (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
- K830660: Sterile Surgical Drapes (Mar 17, 1983)
- K821044: Patient Prep Kits/Trays-Sterile (Jun 23, 1982)
- K821666: Sterile Surgical Drapes (Jun 21, 1982)
- K821043: Sterile Patient Exam. Gloves (May 21, 1982)
- K801846: Electrocardiograph Electrode (Sep 9, 1980)
- K781820: Gloves, Vinyl Examination (Dec 7, 1978)

Source page: https://510kreport.com/company/phoenix-glove