510(k) K223884 ยท QAJ Cutaneous Electrode Stimulator For Urinary Incontinence
ELITONE Urge Urinary Incontinence Device
| Applicant | Elidah, Inc., Monroe CT, US |
| Decision | Substantially Equivalent, Feb 24, 2023 |
| Received | Dec 27, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223884
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.