ClearanceBrief
510(k) K911229 ยท GWQ Full-Montage Standard Electroencephalograph

PHOENIX DIGITAL EEG SYSTEM

ApplicantDantec Medical, Inc., Washington DC, US
DecisionSubstantially Equivalent, Sep 30, 1991
ReceivedMar 20, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911229

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.