ClearanceBrief
510(k) K092890 ยท BZG Spirometer, Diagnostic

ASTHMA MONITOR AM3

ApplicantCarefusion Germany 234 GmbH, Hoechberg, DE
DecisionSubstantially Equivalent, Jan 13, 2010
ReceivedSep 21, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K092890

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.