K-number	K090432
Device name	HEMORPEX SYSTEM
Applicant	Angiologica B. M. Srl
Product code	FER
Device class	Class II
Decision date	May 29, 2009
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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HEMORPEX SYSTEM

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