ClearanceBrief
510(k) K992823 ยท BZG Spirometer, Diagnostic

SPIROVIT SP-2, PNEUMOCHECK II

ApplicantSchiller AG, Baar, CH
DecisionSubstantially Equivalent, May 12, 2000
ReceivedAug 23, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992823

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.