510(k) K192834 ยท QGH Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder
MECTA Sigma
| Applicant | Mecta Corporation, Suite B OR, US |
| Decision | Substantially Equivalent, Apr 26, 2020 |
| Received | Oct 2, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192834
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.