510(k) K071186 ยท IKT Electrode, Needle, Diagnostic Electromyograph
MODIFICATION TO: AMBU NEUROLINE CONCENTRIC NEEDLE ELECTRODE
| Applicant | Ambu A/S, Glen Burnie MD, US |
| Decision | Substantially Equivalent, Jul 30, 2007 |
| Received | Apr 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071186
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.