510(k) K072123 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE
| Applicant | Biowave Corporation, North Attleboro MA, US |
| Decision | Substantially Equivalent, Feb 1, 2008 |
| Received | Aug 2, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072123
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.