# Leocor, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 4 (1990–1992): 3 510(k) clearances and 1 original PMA approval
- Product codes: LOX (1), DXK (1), DQI (1), DQO (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
- K924110: Leocor Corflo Pump -- Modification (Sep 1, 1992)
- K911270: Leocor Guiding Catheter (Jan 17, 1992)
- K900350: Leocor Corflo (TM) Pump (Jul 17, 1990)
- P890001: Leocor,Inc. Models 1 (Mar 30, 1990)

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