K-number	K062421
Device name	MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZER
Applicant	Mentor Corporation
Product code	MRD
Device class	Class U
Decision date	Oct 10, 2006
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZER

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