K253926
- 510(k) number
- K253926
- Device name
- Diacore
- Applicant
- ShenB Co., Ltd. KR
- Product code
- NGX — Stimulator, Muscle, Powered, For Muscle Conditioning
- Decision date
- 2026-04-10
- Date received
- 2025-12-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K253926.pdf
Official FDA record: K253926
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.