510(k) K020803 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
CEFAR MEDICAL AB CEFAR PRIMO
| Applicant | Cefar Medical AB, Minneapolis, MN, US |
| Decision | Substantially Equivalent, Jun 10, 2002 |
| Received | Mar 12, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020803
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.