# Urocor, Inc.

- Location (FDA's records): Oklahoma City, OK
- FDA decisions: 1 (1999–1999): 1 510(k) clearance
- Product codes: KXK (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Medi-Physics Inc. Dba Nycomed Amersham Imaging: 1 (https://510kreport.com/company/medi-physics-dba-nycomed-amersham-imaging)

## Recent decisions
- K984446: `BI I-125 Brachytheraphy Seed, Model 125SL & 125SH (Apr 16, 1999)

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