510(k) K001410 ยท KTB Device, Iontophoresis, Specific Uses
PHORESOR MODEL PM2000
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Aug 1, 2000 |
| Received | May 4, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001410
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.