510(k) K241267 ยท EGJ Device, Iontophoresis, Other Uses
Hidroxa SE30
| Applicant | Hidroxa Medical AB, Partille, SE |
| Decision | Substantially Equivalent, Oct 17, 2024 |
| Received | May 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241267
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.