K-number	K920128
Device name	VERSACATH MAINLINE CENTRAL VENOUS CATHETER
Applicant	Menlo Care, Inc.
Product code	FOZ
Device class	Class II
Decision date	Mar 26, 1992
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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VERSACATH MAINLINE CENTRAL VENOUS CATHETER

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