510(k) K172503 ยท GXY Electrode, Cutaneous
MR Conditional Cup Electrode, MR Conditional Webb Electrode
| Applicant | Rhythmlink International, LLC, Columbia SC, US |
| Decision | Substantially Equivalent, Dec 1, 2017 |
| Received | Aug 18, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172503
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.