ClearanceBrief
510(k) K902550 ยท GWQ Full-Montage Standard Electroencephalograph

EEG-5400 SERIES

ApplicantNihon Kohden America, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Mar 19, 1991
ReceivedJun 6, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902550

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.