K-number	K013638
Device name	MODIFICATION TO VIKING OPTIMA GUIDING CATHETER
Applicant	Guidant Corp.
Product code	DQY
Device class	Class II
Decision date	Dec 4, 2001
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO VIKING OPTIMA GUIDING CATHETER

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