510(k) K001117 ยท GXY Electrode, Cutaneous
COMFORT STIM
| Applicant | R & D Medical Products, Inc., Lake Forest CA, US |
| Decision | Substantially Equivalent, Jul 5, 2000 |
| Received | Apr 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001117
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.