K-number	K071543
Device name	HALO360' COAGULATION CATHETER
Applicant	Barrx Medical, Incorporated
Product code	GEI
Device class	Class II
Decision date	Jun 29, 2007
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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HALO360' COAGULATION CATHETER

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