ClearanceBrief
510(k) K970596 ยท BWF Spirometer, Therapeutic (Incentive)

DHD EMERALD PRODUCT

ApplicantDhd Diemolding Healthcare Div., Wampsville NY, US
DecisionSubstantially Equivalent, May 16, 1997
ReceivedFeb 18, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970596

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.