ClearanceBrief
510(k) K161536 ยท BZG Spirometer, Diagnostic

EasyOne Air Spirometer

ApplicantNdd Medizintechnik AG, Zurich, CH
DecisionSubstantially Equivalent, Jan 5, 2017
ReceivedJun 3, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K161536

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.