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Gynetech Pty. , Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K150519ManipulatOR PRO, ManipulatORAugust 19, 2015
K142700InsufflatOR NeedleDecember 19, 2014
K142164MANIPULATOR; MANIPULATOR PRODecember 17, 2014
K051594MCCARTNEY ACCESS TUBESeptember 2, 2005