ClearanceBrief
510(k) K832401 ยท BZG Spirometer, Diagnostic

RESPIROMETER

ApplicantKinetix, Walker MI, US
DecisionSubstantially Equivalent, Apr 30, 1984
ReceivedJul 20, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832401

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.