ClearanceBrief
510(k) K031102 ยท BZG Spirometer, Diagnostic

MICROLAB SPIROMETER

ApplicantMicro Direct, Inc., Lewiston ME, US
DecisionSubstantially Equivalent, Dec 1, 2003
ReceivedApr 7, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031102

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.