510(k) K831320 ยท EGJ Device, Iontophoresis, Other Uses
DRIONIC
| Applicant | General Medical Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 19, 1983 |
| Received | Apr 22, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831320
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.