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Iogyn, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K141848IOGYN SYSTEMAugust 29, 2014
DEN130040IOGYN SYSTEMMarch 28, 2014
K123330IOGYN ENDOSCOPEMarch 19, 2013