510(k) K062880 ยท GXZ Electrode, Needle
SUBDERMAL WIRE ELECTRODE, MODEL SWE
| Applicant | Ives Eeg Solutions, Inc., Manotick, Ontario, CA |
| Decision | Substantially Equivalent, Dec 22, 2006 |
| Received | Sep 26, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062880
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.