510(k) K140530 ยท BWK Stimulator, Electro-Acupuncture
Electro Auricular Device
| Applicant | Navigant Consulting, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Oct 2, 2014 |
| Received | Mar 4, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140530
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.