510(k) K896444 ยท EGJ Device, Iontophoresis, Other Uses
IONTOPHORESIS DEVICE - ELECTRODE RH 800
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Unknown, May 10, 1990 |
| Received | Nov 9, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896444
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.