K-number	K010853
Device name	GUIDER SOFTIP GUIDING CATHETER XF 5F
Applicant	Boston Scientific, Target
Product code	DQY
Device class	Class II
Decision date	Apr 18, 2001
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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GUIDER SOFTIP GUIDING CATHETER XF 5F

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