510(k) K863815 ยท QGH Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder
ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000
| Applicant | Elcot, Inc., New York NY, US |
| Decision | Substantially Equivalent, Jun 2, 1987 |
| Received | Sep 30, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863815
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.