510(k) K914621 ยท EGJ Device, Iontophoresis, Other Uses
IONTOPHORESIS DEVICE, MODIFICATION
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Unknown, Dec 20, 1991 |
| Received | Sep 11, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914621
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.