# Quali-Med, Inc.

- Location (FDA's records): Sugar Land, TX
- FDA decisions: 7 (1986–1987): 7 510(k) clearances
- Product codes: GEX (1), FRG (1), HHT (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
- K871408: Blood Vessel Connector (Apr 27, 1987)
- K862972: Disposable Mirror (Sep 23, 1986)
- K862472: Quartz Rods Titanium Rods (Sep 12, 1986)
- K862241: Standard Basin Kit  Custom Basin Kit (Aug 1, 1986)
- K862242: Pap Smear Kit (Jun 26, 1986)
- K862172: Quali-Med's Operating Room Drapes (Jun 19, 1986)
- K861198: Custom Procedure Kit (Various Sub-Titles) (May 16, 1986)

Source page: https://510kreport.com/company/quali-med