ClearanceBrief
510(k) K051864 ยท GWF Stimulator, Electrical, Evoked Response

MAGSTIM RAPID2, MAGSTIM SUPER RAPID2, MODELS 3004-000, 3005-00

ApplicantThe Magstim Company , Ltd., Whitland, Dyfed Wales, GB
DecisionSubstantially Equivalent, Dec 21, 2005
ReceivedJul 8, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051864

DateFirm and productCodeLinked 510(k)
Mar 23, 2020The Magstim Company Limited
Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from p
Terminated
OBPNone listed
Mar 23, 2020The Magstim Company Limited
Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antid
Terminated
OBPNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.