510(k) K934335 ยท EGJ Device, Iontophoresis, Other Uses
PHORESOR II AUTO, MODEL PM800 MODIFICATION
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 26, 1994 |
| Received | Sep 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934335
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.