510(k) K943449 ยท GXY Electrode, Cutaneous
NEUROLOGICAL DIAGNOSTIC DEVICES
| Applicant | Henley Intl., Sugar Land TX, US |
| Decision | Substantially Equivalent, Nov 15, 1995 |
| Received | Jul 18, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943449
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.