ClearanceBrief
510(k) K913726 ยท BZA Connector, Airway (Extension)

DURALIFE(TM)

ApplicantDhd Diemolding Healthcare Div., Canastota NY, US
DecisionSubstantially Equivalent, Feb 7, 1992
ReceivedAug 20, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913726

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.