ClearanceBrief
510(k) K902607 ยท GWF Stimulator, Electrical, Evoked Response

DANTEC MAGNETIC STIMULATOR MAG 2 (MAG 2)

ApplicantDantec Medical, Inc., Washington DC, US
DecisionSubstantially Equivalent, May 14, 1991
ReceivedJun 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902607

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.