510(k) K915444 ยท EGJ Device, Iontophoresis, Other Uses
DUPEL IONTOPHORESIS DEVICE
| Applicant | Empi, Arden Hills MN, US |
| Decision | Substantially Equivalent, Jul 15, 1994 |
| Received | Dec 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915444
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.