510(k) K093825 ยท IKT Electrode, Needle, Diagnostic Electromyograph
AMBU NEUROLINE DISPOSABLE INOJECT NEEDLE ELECTRODE
| Applicant | Ambu A/S, Glen Burnie MD, US |
| Decision | Substantially Equivalent, Jan 13, 2010 |
| Received | Dec 14, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093825
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.