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Ecleris USA

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K131323ECLERIS SINUSCOPEJune 9, 2014
K100595ECLERIS MICROSTAR COLPOSCOPEJuly 9, 2010