K-number	K083690
Device name	FEMVUE(TM) CATHETER SYSTEM
Applicant	Femasys, Inc.
Product code	LKF
Device class	Class II
Decision date	Jun 23, 2009
Decision	Substantially Equivalent
Regulation	884.4530

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View the full FDA submission: accessdata.fda.gov

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FEMVUE(TM) CATHETER SYSTEM

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