K-number	K102815
Device name	SURELIFT PROLAPSE SYSTEM
Applicant	Neomedic International
Product code	OTP
Device class	Class III
Decision date	Jul 7, 2011
Decision	Substantially Equivalent
Regulation	884.5980

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Source

View the full FDA submission: accessdata.fda.gov

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SURELIFT PROLAPSE SYSTEM

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