510(k) K935868 ยท EGJ Device, Iontophoresis, Other Uses
DYNAPHOR(TM) TWO
| Applicant | Maxxim Medical, Sugar Land TX, US |
| Decision | Substantially Equivalent, Mar 15, 1995 |
| Received | Dec 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935868
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.