ClearanceBrief
510(k) K963035 ยท BZG Spirometer, Diagnostic

MICRO SPIROMETER

ApplicantMicro Direct, Inc., Auburn ME, US
DecisionSubstantially Equivalent, Nov 1, 1996
ReceivedAug 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963035

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.