K-number	K953909
Device name	SCIMED 6 FRENCH MICRO-MAX GUIDE CATHETER
Applicant	Scimed
Product code	DQY
Device class	Class II
Decision date	Nov 13, 1995
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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SCIMED 6 FRENCH MICRO-MAX GUIDE CATHETER

Everything you need for a 510(k) submission. Nothing you don't.