ClearanceBrief
510(k) K120577 ยท BZG Spirometer, Diagnostic

MEDIKRO SPIROSTAR, M929 Medikro Spirostar USB and M921 Medikro SpiroStar DX

ApplicantMedikro OY, Kuopio, FI
DecisionSubstantially Equivalent, Jun 24, 2015
ReceivedFeb 27, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120577

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.