K-number	K024107
Device name	FEMOSTOP FEMORAL COMPRESSION SYSTEM
Applicant	Radi Medical Systems AB
Product code	DXC
Device class	Class II
Decision date	Dec 24, 2002
Decision	Substantially Equivalent
Regulation	870.4450

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View the full FDA submission: accessdata.fda.gov

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FEMOSTOP FEMORAL COMPRESSION SYSTEM

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