ClearanceBrief
510(k) K933951 ยท GWQ Full-Montage Standard Electroencephalograph

VIDEO EEG OPTION MODIFICATION

ApplicantEsaote Biomedica Spa, Indianapolis IN, US
DecisionSubstantially Equivalent, Feb 3, 1994
ReceivedAug 12, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933951

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.