510(k) K022405 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MIC
| Applicant | Rehabilicare, Inc., New Brighton MN, US |
| Decision | Substantially Equivalent, Aug 12, 2002 |
| Received | Jul 16, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022405
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.