510(k) K043047 ยท EGJ Device, Iontophoresis, Other Uses
DYNATRON IBOX IONTOPHORESIS DEVICE
| Applicant | Dynatronics Corp., Salt Lake City UT, US |
| Decision | Unknown, Jan 7, 2005 |
| Received | Nov 4, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043047
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.