510(k) K883869 ยท GYA Tester, Electrode/Lead, Electroencephalograph
DERMTRODE
| Applicant | World Precision Instruments, Inc., New Haven CT, US |
| Decision | Substantially Equivalent, Sep 30, 1988 |
| Received | Sep 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883869
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.