# Bicore Monitoring Systems

- Location (FDA's records): Irvine, CA
- FDA decisions: 4 (1990–1995): 4 510(k) clearances
- Product codes: BZK (1), BZC (1), BYR (1), MOD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- Bear Medical Systems, Inc.: 2 (https://510kreport.com/company/bear-medical-systems)
- Respironics Novametrix, Inc.: 1 (https://510kreport.com/company/respironics-novametrix)
- Maquet Critical Care AB: 1 (https://510kreport.com/company/maquet-critical-care)

## Its most-cited devices
- K900696: Biore CP-100 Cardiopulmonary Monitor (1990), cited by 2
- K935788: Bicore Smartcath Intratracheal Catheter (1995), cited by 2

## Recent decisions
- K935788: Bicore Smartcath Intratracheal Catheter (Jul 3, 1995)
- K921717: Bicore Smartvalve Occlusion Valve (Nov 6, 1992)
- K900696: Biore CP-100 Cardiopulmonary Monitor (Nov 29, 1990)
- K896718: Bicore Variflex (R) Flow Transducer (Feb 22, 1990)

Source page: https://510kreport.com/company/bicore-monitoring-systems