K-number	K151254
Device name	CARDIOSAVE Hybrid Intra-Aortic Balloon Pump
Applicant	Datascope Corp.
Product code	DSP
Device class	Class II
Decision date	Jul 2, 2015
Decision	Substantially Equivalent
Regulation	870.3535

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View the full FDA submission: accessdata.fda.gov

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CARDIOSAVE Hybrid Intra-Aortic Balloon Pump

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