510(k) K925806 ยท EGJ Device, Iontophoresis, Other Uses
RH-801, MODEL TRANSQ
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 14, 1994 |
| Received | Nov 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925806
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.