ClearanceBrief
510(k) K133722 ยท BZG Spirometer, Diagnostic

ASTHMA MONITOR AM3

ApplicantEresearch Technology, Philadelphia PA, US
DecisionSubstantially Equivalent, May 8, 2014
ReceivedDec 5, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133722

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.