ClearanceBrief
510(k) K842139 ยท KPM Shunt, Peritoneal

THE DENVER PLEURAL-PERITONEAL SHUNT

ApplicantDenver Biomedicals, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 27, 1984
ReceivedMay 30, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842139

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.