ClearanceBrief
510(k) K920877 ยท BZG Spirometer, Diagnostic

THE KEYSTONE SYSTEM

ApplicantS & M Instrument Co., Doylestown PA, US
DecisionSubstantially Equivalent, Dec 23, 1992
ReceivedFeb 26, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920877

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.