510(k) DEN250013 ยท SHX Transcranial Nerve Stimulation Device For The Treatment Of Post-Traumatic Stress Disorder Associated Symptoms
Modius Spero
| Applicant | Neurovalens Limited, Portglenone, GB |
| Decision | Unknown, May 8, 2026 |
| Received | Apr 16, 2025 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN250013
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.