510(k) K032278 ยท GXY Electrode, Cutaneous
AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE
| Applicant | Ambu, Inc., Linthicum MD, US |
| Decision | Substantially Equivalent, Mar 5, 2004 |
| Received | Jul 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032278
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.