ClearanceBrief
510(k) K083233 ยท BZG Spirometer, Diagnostic

THE PFT FILTER

ApplicantPulmonary Filtration Technologies, LLC, Bonita Springs FL, US
DecisionSubstantially Equivalent, Mar 2, 2009
ReceivedNov 3, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083233

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.