ClearanceBrief
510(k) K803037 ยท DWM Apparatus, Suction, Patient Care

WILLIAM HARVEY VENTED MEDIASTINAL DRAIN

ApplicantC.R. Bard, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 4, 1981
ReceivedDec 1, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K803037

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.