510(k) K083016 ยท EGJ Device, Iontophoresis, Other Uses
ACTHYDERM
| Applicant | Microlab Americas, Inc., Crofton MD, US |
| Decision | Substantially Equivalent, Jun 16, 2009 |
| Received | Oct 9, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083016
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.