510(k) K001522 ยท KTB Device, Iontophoresis, Specific Uses
TRANSQ3
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 18, 2000 |
| Received | May 16, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001522
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.