ClearanceBrief
510(k) K965042 ยท BZG Spirometer, Diagnostic

MICRODL DIARYCARD SPIROMETER

ApplicantMicro Direct, Inc., Auburn ME, US
DecisionSubstantially Equivalent, Jun 17, 1997
ReceivedDec 17, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K965042

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.