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Bicore Monitoring Systems

FDA Regulatory Profile

Bicore Monitoring Systems appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 3, 1995.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K935788BICORE SMARTCATH INTRATRACHEAL CATHETERJuly 3, 1995
K921717BICORE SMARTVALVE OCCLUSION VALVENovember 6, 1992
K900696BIORE CP-100 CARDIOPULMONARY MONITORNovember 29, 1990
K896718BICORE VARIFLEX(R) FLOW TRANSDUCERFebruary 22, 1990

FDA data resources