510(k) K132832 ยท EGJ Device, Iontophoresis, Other Uses
ACTIVAPATCH ET IONTOPHORESIS PATCH
| Applicant | Activatek, Inc., West Valley City UT, US |
| Decision | Substantially Equivalent, Feb 13, 2014 |
| Received | Sep 10, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132832
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.