510(k) K091326 ยท EGJ Device, Iontophoresis, Other Uses
ACTIVAPATCH
| Applicant | Activatek, Inc., West Valley UT, US |
| Decision | Substantially Equivalent, May 27, 2009 |
| Received | May 5, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091326
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.