510(k) K853898 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
SKYLARK MODEL 1001 TENS DEVICE
| Applicant | Peleg Intl. Co., Canada, CA |
| Decision | Substantially Equivalent, Jun 18, 1986 |
| Received | Sep 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853898
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.