ClearanceBrief
510(k) K913957 ยท GWJ Stimulator, Auditory, Evoked Response

DANTEC COUNTERPOINT MK2(TM)

ApplicantDantec Medical, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jan 30, 1992
ReceivedSep 4, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913957

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.