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Optical Sensors, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K040654SENSILASE PAD 3000June 4, 2004
K010795CAPNOPROBE SL, MODEL 2000April 11, 2001
K984579CAPNO PROBE ADecember 21, 2000
K961790POINT-OF-CARE BLOOD GAS MONITOR SYSTEMApril 9, 1997
K963935OLYMPUS CRITICAL CARE MONITORING SYSTEMJanuary 23, 1997
K951094POINT-OF-CARE ARTERIAL BLOOD GAS MONITORING SYSTEMJanuary 16, 1996
K931185SENSICATH POINT-OF-CARE BLOOD GAS MONITORING SYSTEOctober 21, 1993