ClearanceBrief
510(k) K912234 ยท BZG Spirometer, Diagnostic

SOMNIPROBE(R) MODEL NUMBER 10093, MODIFICATION

ApplicantSomnitec, Inc., Van Nuys CA, US
DecisionSubstantially Equivalent, Jul 22, 1991
ReceivedMay 17, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912234

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.