510(k) K860467 ยท QGH Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder
ELECTROSHOCK UNIT NEUROLOGY MODEL B-25
| Applicant | Medcraft Corp., Darien CT, US |
| Decision | Substantially Equivalent, Nov 10, 1986 |
| Received | Feb 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860467
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.