510(k) K031115 ยท KTB Device, Iontophoresis, Specific Uses
RH-900
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 10, 2003 |
| Received | Apr 8, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031115
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.