K-number	K094048
Device name	PERCUPRO MESSENGER BALLOON CATHETER
Applicant	Cardiosolutions, Inc.
Product code	DYG
Device class	Class II
Decision date	Jul 14, 2011
Decision	Substantially Equivalent
Regulation	870.1240

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Source

View the full FDA submission: accessdata.fda.gov

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PERCUPRO MESSENGER BALLOON CATHETER

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