K-number	K082935
Device name	VISION WIRE CORONARY GUIDEWIRE
Applicant	Biotronik, Inc.
Product code	DQX
Device class	Class II
Decision date	Dec 4, 2008
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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VISION WIRE CORONARY GUIDEWIRE

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