510(k) K010638 ยท GXY Electrode, Cutaneous
NEUROPLUS, MODEL A10040, A10041, A10042, A10043
| Applicant | Vermont Medical, Inc., Bellows Falls VT, US |
| Decision | Substantially Equivalent, May 3, 2001 |
| Received | Mar 5, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010638
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.