510(k) K960754 ยท QGH Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder
SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M
| Applicant | Mecta Corp., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Sep 18, 1996 |
| Received | Feb 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960754
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.