ClearanceBrief
510(k) K945120 ยท QGH Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder

THYMATRON 2000 ELECTROCONVULSIVE SYSTEM

ApplicantSomatics, Inc., Lake Bluff IL, US
DecisionSubstantially Equivalent, Oct 26, 1995
ReceivedOct 19, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945120

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.