K-number	K904680
Device name	THERATEK GROUP EXCHANGE CATHETER
Applicant	Dow Corning Wright
Product code	MCW
Device class	Class II
Decision date	Dec 27, 1990
Decision	Substantially Equivalent
Regulation	870.4875

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View the full FDA submission: accessdata.fda.gov

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THERATEK GROUP EXCHANGE CATHETER

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