510(k) K883914 ยท GWE Stimulator, Photic, Evoked Response
FATIGMETER
| Applicant | K. Jimbo Co., Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Oct 31, 1989 |
| Received | Sep 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883914
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.