510(k) K060236 ยท EGJ Device, Iontophoresis, Other Uses
MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 31, 2006 |
| Received | Jan 30, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060236
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.