510(k) K903093 ยท EGJ Device, Iontophoresis, Other Uses
IONTOPHORESIS DEVICE
| Applicant | Empi, Arden Hills MN, US |
| Decision | Unknown, Oct 11, 1990 |
| Received | Jul 13, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903093
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.