K-number	K131853
Device name	MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER
Applicant	Mentor Worldwide, LLC
Product code	MRD
Device class	Class U
Decision date	Jul 17, 2013
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER

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