Bicore Monitoring Systems
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K935788 | BICORE SMARTCATH INTRATRACHEAL CATHETER | July 3, 1995 |
| K921717 | BICORE SMARTVALVE OCCLUSION VALVE | November 6, 1992 |
| K900696 | BIORE CP-100 CARDIOPULMONARY MONITOR | November 29, 1990 |
| K896718 | BICORE VARIFLEX(R) FLOW TRANSDUCER | February 22, 1990 |