ClearanceBrief
510(k) K012235 ยท KPM Shunt, Peritoneal

DENVER PLEURAL EFFUSION SHUNT AND DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER

ApplicantDenver Biomedical, Inc., Golden CO, US
DecisionSubstantially Equivalent, Oct 4, 2001
ReceivedJul 17, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K012235

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.