ClearanceBrief
510(k) K222443 ยท BZG Spirometer, Diagnostic

Air Smart Extra Spirometer

ApplicantFeellife Health, Inc., Shenzhen, CN
DecisionSubstantially Equivalent, Aug 9, 2023
ReceivedAug 12, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222443

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.