ClearanceBrief
510(k) K010642 ยท DWM Apparatus, Suction, Patient Care

PLEURX PLEURAL CATHETER AND DRAINAGE KITS

ApplicantDenver Biomedicals, Inc., Golden CO, US
DecisionSubstantially Equivalent, Mar 20, 2001
ReceivedMar 5, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010642

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.