510(k) K982668 ยท EGJ Device, Iontophoresis, Other Uses
PHORESOR II,MODEL PM900
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 2, 1999 |
| Received | Jul 31, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982668
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.