ClearanceBrief
510(k) K926516 ยท GWF Stimulator, Electrical, Evoked Response

DANTEC MAGNETIC STIMULATOR MAGPRO

ApplicantDantec Medical, Inc., Washington DC, US
DecisionSubstantially Equivalent, Aug 31, 1993
ReceivedDec 30, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926516

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.