K-number	K121301
Device name	XPRESSWAY RX CATHETER (6F LD-VERISON)
Applicant	Kaneka Pharma America, LLC
Product code	QEZ
Device class	Class II
Decision date	Jul 30, 2012
Decision	Substantially Equivalent
Regulation	870.5150

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View the full FDA submission: accessdata.fda.gov

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XPRESSWAY RX CATHETER (6F LD-VERISON)

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