K-number	K925131
Device name	CORDIS 9 F GUIDING CATHETER
Applicant	Cordis Corp.
Product code	DQY
Device class	Class II
Decision date	May 6, 1993
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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CORDIS 9 F GUIDING CATHETER

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