510(k) K051529 ยท GXY Electrode, Cutaneous
AMBU NEUROLINE GROUND
| Applicant | Ambu, Inc., Glen Burnie MD, US |
| Decision | Substantially Equivalent, Aug 4, 2005 |
| Received | Jun 9, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051529
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.