K-number	K010709
Device name	MENTOR STERILE SALINE MAMMARY VOLUME SIZERS
Applicant	Mentor Corp.
Product code	MRD
Device class	Class U
Decision date	Apr 23, 2001
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MENTOR STERILE SALINE MAMMARY VOLUME SIZERS

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