510(k) K913522 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
SOLITENS MODIFIED
| Applicant | Innovative Designer Products, Inc., Glen Rock NJ, US |
| Decision | Substantially Equivalent, Aug 28, 1991 |
| Received | Jul 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913522
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.