510(k) K020476 ยท EGJ Device, Iontophoresis, Other Uses
MEDION 6000
| Applicant | Selectivemed Components, Inc., Mount Vernon OH, US |
| Decision | Substantially Equivalent, May 3, 2002 |
| Received | Feb 12, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020476
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.