Bicore Monitoring Systems - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Bicore Monitoring Systems has 4 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 4 cleared submissions from 1990 to 1995. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Bicore Monitoring Systems Filter by specialty or product code using the sidebar.
4 devices
Cleared
Jul 03, 1995
BICORE SMARTCATH INTRATRACHEAL CATHETER
Anesthesiology
574d
Cleared
Nov 06, 1992
BICORE SMARTVALVE OCCLUSION VALVE
Anesthesiology
211d
Cleared
Nov 29, 1990
BIORE CP-100 CARDIOPULMONARY MONITOR
Anesthesiology
289d
Cleared
Feb 22, 1990
BICORE VARIFLEX(R) FLOW TRANSDUCER
Anesthesiology
85d