K-number	K921311
Device name	CORDIS SHUTTLE CATHETER W/ SIDEHOLES
Applicant	Cordis Corp.
Product code	DQY
Device class	Class II
Decision date	Sep 9, 1992
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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CORDIS SHUTTLE CATHETER W/ SIDEHOLES

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