ClearanceBrief
510(k) K831324 ยท GWQ Full-Montage Standard Electroencephalograph

EEG 42/2P ELECTRO ENCEPHALOGRAPH

ApplicantNihon Kohden America, Inc., Foothill CA, US
DecisionSubstantially Equivalent, May 27, 1983
ReceivedApr 25, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831324

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.