ClearanceBrief
510(k) K910452 ยท BZG Spirometer, Diagnostic

RESPI-PAK RT-PAK

ApplicantCns, Inc., Eden Prairie MN, US
DecisionSubstantially Equivalent, Apr 16, 1991
ReceivedFeb 1, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910452

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.