510(k) K062198 ยท GXY Electrode, Cutaneous
SUNSPOTS PRE-GELLED SURFACE ELECTRODES
| Applicant | Axon Systems, Inc., Hauppauge NY, US |
| Decision | Substantially Equivalent, Dec 19, 2006 |
| Received | Aug 1, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062198
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.