510(k) K843923 ยท QGH Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder
THYMATRON
| Applicant | Somatics, Inc., Lake Bluff IL, US |
| Decision | Substantially Equivalent, Dec 3, 1984 |
| Received | Oct 5, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843923
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.