K-number	K150519
Device name	ManipulatOR PRO, ManipulatOR
Applicant	Gynetech Pty. , Ltd.
Product code	LKF
Device class	Class II
Decision date	Aug 19, 2015
Decision	Substantially Equivalent
Regulation	884.4530

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View the full FDA submission: accessdata.fda.gov

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ManipulatOR PRO, ManipulatOR

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