ClearanceBrief
510(k) K897094 ยท BZG Spirometer, Diagnostic

MODIFIED SPIROSCAN 1000

ApplicantFukuda Denshi USA, Inc., Redmond WA, US
DecisionSubstantially Equivalent, Jan 12, 1990
ReceivedDec 20, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K897094

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.