K-number	K092372
Device name	HEARTRAIL III GUIDING CATHETER
Applicant	Terumo Corp.
Product code	DQO
Device class	Class II
Decision date	Sep 11, 2009
Decision	Substantially Equivalent
Regulation	870.1200

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View the full FDA submission: accessdata.fda.gov

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HEARTRAIL III GUIDING CATHETER

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