K-number	K023051
Device name	INTRAUTERINE DELIVERY SYSTEM - INJECTOR
Applicant	Prosurg, Inc.
Product code	LKF
Device class	Class II
Decision date	Dec 12, 2002
Decision	Substantially Equivalent
Regulation	884.4530

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View the full FDA submission: accessdata.fda.gov

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INTRAUTERINE DELIVERY SYSTEM - INJECTOR

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