ClearanceBrief
510(k) K020400 ยท GWF Stimulator, Electrical, Evoked Response

DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR

ApplicantMeps, LLC, Fort Lauderdale FL, US
DecisionSubstantially Equivalent, Aug 23, 2002
ReceivedFeb 6, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020400

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.