K252767
- 510(k) number
- K252767
- Device name
- actiTENS mini
- Applicant
- Sublimed FR
- Product code
- GZJ — Stimulator, Nerve, Transcutaneous, For Pain Relief
- Decision date
- 2026-01-16
- Date received
- 2025-08-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K252767.pdf
Official FDA record: K252767
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.