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Oricare, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K131790A9800 ANESTHESIA WORKSTATIONMay 9, 2014
K120931CRITICAL CARE VENTILATORJune 6, 2013
K122875ORICARE L2700December 18, 2012
K113338MEDICAL AIR COMPRESSORAugust 10, 2012