ClearanceBrief
510(k) K820036 ยท BZG Spirometer, Diagnostic

CXD 400

ApplicantCdx Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 22, 1982
ReceivedJan 7, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820036

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.