THE DENVER PLEURAL-PERITONEAL SHUNT— 510(k) K842139

Substantially Equivalent

Denver Biomedicals, Inc.

FDA 510(k) clearance K842139 for THE DENVER PLEURAL-PERITONEAL SHUNT, Substantially Equivalent on 1984-08-27. Applicant: Denver Biomedicals, Inc..

Clearance details

Applicant: Denver Biomedicals, Inc.
Product code: Code KPM
Advisory panel: Gastroenterology, Urology
Date received: 1984-05-30
Decision date: 1984-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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