510(k) K894549 ยท EGJ Device, Iontophoresis, Other Uses
DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE
| Applicant | Henley Intl., Sugar Land TX, US |
| Decision | Unknown, Feb 9, 1990 |
| Received | Jul 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894549
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.