K-number	K071281
Device name	UNIRING - ANNULOPLASTY RING WITH SIZERS
Applicant	Peters Surgical
Product code	KRH
Device class	Class II
Decision date	Aug 3, 2007
Decision	Substantially Equivalent
Regulation	870.3800

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View the full FDA submission: accessdata.fda.gov

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UNIRING - ANNULOPLASTY RING WITH SIZERS

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