K-number	K090051
Device name	LEVITRONIX PEDIMAG BLOOD PUMP, MODEL 201-90052
Applicant	Levitronix, LLC
Product code	KFM
Device class	Class II
Decision date	Oct 8, 2009
Decision	Substantially Equivalent
Regulation	870.4360

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View the full FDA submission: accessdata.fda.gov

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LEVITRONIX PEDIMAG BLOOD PUMP, MODEL 201-90052

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