510(k) K080386 ยท GXY Electrode, Cutaneous
COLUMBIA 600 ELECTRODE, COLUMBIA 06 LEADWIRE
| Applicant | Columbia Scientific Development, LLC, Portland OR, US |
| Decision | Substantially Equivalent, May 30, 2008 |
| Received | Feb 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080386
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.