# Keystone Medical

- Location (FDA's records): Great Neck, NY
- FDA decisions: 2 (2000–2001): 2 510(k) clearances
- Product codes: FOZ (1), MPB (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
- Medcomp: 1 (https://510kreport.com/company/medcomp)

## Recent decisions
- K011860: KEYST0NE Medical Picc Catheter (Jun 27, 2001)
- K001958: Keystone Medical Schon XL Soft-Line Double Lument Catheter. Keystone Medical 12 F Duo-Flow and 14F Duo-Flow 400 XL Cath (Sep 25, 2000)

Source page: https://510kreport.com/company/keystone-medical
