K-number	K112892
Device name	IMPELLA 2.5 PLUS CATHETER
Applicant	Abiomed, Inc.
Product code	PBL
Device class	Class unclassified
Decision date	Sep 6, 2012
Decision	Unknown
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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IMPELLA 2.5 PLUS CATHETER

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