ClearanceBrief
510(k) K130322 ยท BZG Spirometer, Diagnostic

SPM-300

ApplicantBionet Co., Ltd., Irvine CA, US
DecisionSubstantially Equivalent, Nov 15, 2013
ReceivedFeb 8, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130322

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.