ClearanceBrief
510(k) K781922 ยท BZH Meter, Peak Flow, Spirometry

PULMONARY MONITOR

ApplicantVitalograph , Ltd., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 13, 1979
ReceivedNov 13, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781922

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.