ClearanceBrief
510(k) K823922 ยท BZK Spirometer, Monitoring (W/Wo Alarm)

COMPUTERIZED SPIROMETRY SYSTEM

ApplicantOhio Medical Products, Mchenry IL, US
DecisionSubstantially Equivalent, Feb 24, 1983
ReceivedDec 28, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823922

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.