K-number	K844889
Device name	MENSINK-GOOSEN CATHETER
Applicant	Goosen Enterprises, Inc.
Product code	GBP
Device class	Class I
Decision date	Mar 18, 1985
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MENSINK-GOOSEN CATHETER

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