510(k) K011017 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT
| Applicant | Rehabilicare, Inc., New Brighton MN, US |
| Decision | Substantially Equivalent, Sep 24, 2001 |
| Received | Apr 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011017
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.