K-number	K842139
Device name	THE DENVER PLEURAL-PERITONEAL SHUNT
Applicant	Denver Biomedicals, Inc.
Product code	KPM
Device class	Class II
Decision date	Aug 27, 1984
Decision	Substantially Equivalent
Regulation	876.5955

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View the full FDA submission: accessdata.fda.gov

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THE DENVER PLEURAL-PERITONEAL SHUNT

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