510(k) K852069 ยท QGH Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder
MECTA ECT DEVICE MODELS SR & JR
| Applicant | Mecta Corp., Portland OR, US |
| Decision | Substantially Equivalent, Aug 9, 1985 |
| Received | May 10, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852069
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.