ClearanceBrief
510(k) K923950 ยท GWQ Full-Montage Standard Electroencephalograph

THE GALILEO VEGA-24 ELECTROENCEPHALOGRAPH

ApplicantBiosound, Inc., Indianapolis IN, US
DecisionSubstantially Equivalent, Jan 26, 1993
ReceivedAug 5, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923950

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.