# Medicorp, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 5 (1979–1986): 5 510(k) clearances
- Product codes: LIF (2), HST (1), FLC (1), FKQ (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
- K860026: Ultramax Iii, Dialyzer Reprocessing Device (Mar 14, 1986)
- K844850: Medicorp Dehydracon a Dehydrated Dialysate Concent (Apr 2, 1985)
- K832705: Ultramax (Jun 25, 1984)
- K791164: Negatove Pressure Convertor (Oct 4, 1979)
- K791396: Medi-Trak Portable Traction Device (Aug 16, 1979)

Source page: https://510kreport.com/company/medicorp