K-number	K954390
Device name	CORDIS WESTER STAR CATHETER
Applicant	Cordis Webster, Inc.
Product code	DRF
Device class	Class II
Decision date	Dec 21, 1995
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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CORDIS WESTER STAR CATHETER

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