510(k) K932620 ยท EGJ Device, Iontophoresis, Other Uses
RH-806/GS MODEL TRANSQ(R)2
| Applicant | Iomed, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 26, 1994 |
| Received | Jun 1, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932620
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.