ClearanceBrief
510(k) K870432 ยท GWQ Full-Montage Standard Electroencephalograph

A1-A2 AMBULATORY EEG CASSETTE RECORDER

ApplicantGrass-Telefactor Product Group, W. Conshohocken PA, US
DecisionSubstantially Equivalent, May 8, 1987
ReceivedFeb 3, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870432

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.