K-number	K890099
Device name	MODIFIED VAS-CATH CATHETER REPAIR KIT
Applicant	Vas-Cath, Inc.
Product code	LFJ
Device class	Class II
Decision date	Apr 11, 1989
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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MODIFIED VAS-CATH CATHETER REPAIR KIT

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