ClearanceBrief
510(k) K984031 ยท BZG Spirometer, Diagnostic

SPIROVIT, MODEL SP-250

ApplicantSchiller AG, Baar, CH
DecisionSubstantially Equivalent, Apr 30, 1999
ReceivedNov 12, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984031

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.