510(k) K170291 ยท EGJ Device, Iontophoresis, Other Uses
IontoDC
| Applicant | Soterix Medical, Inc., New York NY, US |
| Decision | Substantially Equivalent, May 1, 2017 |
| Received | Jan 31, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170291
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.