ClearanceBrief
510(k) K915096 ยท GWQ Full-Montage Standard Electroencephalograph

NEUROFAX EEG 5532

ApplicantNihon Kohden America, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Mar 11, 1992
ReceivedNov 12, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915096

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.