510(k) K974855 ยท KTB Device, Iontophoresis, Specific Uses
PHORESOR II, MODEL PM900
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent for Some Indications, Mar 27, 1998 |
| Received | Dec 29, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974855
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.