K-number	K894756
Device name	DENVER PERITONEO-VENUS SHUNT
Applicant	Codman & Shurtleff, Inc.
Product code	KPM
Device class	Class II
Decision date	Sep 29, 1989
Decision	Substantially Equivalent
Regulation	876.5955

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View the full FDA submission: accessdata.fda.gov

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DENVER PERITONEO-VENUS SHUNT

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