K-number	K915836
Device name	CORDIS 5.0 FRENCH SUPER TORQUE CATHETERS
Applicant	Cordis Corp.
Product code	DQO
Device class	Class II
Decision date	Feb 11, 1992
Decision	Substantially Equivalent
Regulation	870.1200

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View the full FDA submission: accessdata.fda.gov

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CORDIS 5.0 FRENCH SUPER TORQUE CATHETERS

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