510(k) K120398 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
WITOUCH PRO
| Applicant | Hollywog, LLC, Chattanooga TN, US |
| Decision | Substantially Equivalent, Aug 16, 2012 |
| Received | Feb 8, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120398
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.