K-number	K142164
Device name	MANIPULATOR; MANIPULATOR PRO
Applicant	Gynetech Pty. , Ltd.
Product code	LKF
Device class	Class II
Decision date	Dec 17, 2014
Decision	Substantially Equivalent
Regulation	884.4530

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Source

View the full FDA submission: accessdata.fda.gov

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MANIPULATOR; MANIPULATOR PRO

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