510(k) K152437 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
BiowaveHOME Neuromodulation Pain Therapy Device
| Applicant | Biowave Corporation, Norwalk CT, US |
| Decision | Substantially Equivalent, Sep 25, 2015 |
| Received | Aug 27, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K152437
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.