# Oxequip Health Ind.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1979–1983): 5 510(k) clearances
- Product codes: CCL (2), JXL (1), CAI (1), DRM (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
- K833496: Oxygen Monitor/Controller (Dec 16, 1983)
- K812624: Oxequip Conductive & Non Anes. Breath (Oct 26, 1981)
- K811987: Oxy-Quik Mark IV Oxygen Inhalator (Jul 27, 1981)
- K800369: Tri Pac Mouth Prop (Feb 28, 1980)
- K792356: Oxequip Model 34 Med*Star Oxygen Monitor (Dec 4, 1979)

Source page: https://510kreport.com/company/oxequip-health-ind
