K242926
- 510(k) number
- K242926
- Device name
- XBody Go USA, XBody Pro USA
- Applicant
- Xbody Hungary Kft. HU
- Product code
- NGX — Stimulator, Muscle, Powered, For Muscle Conditioning
- Decision date
- 2025-05-30
- Date received
- 2024-09-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K242926.pdf
Official FDA record: K242926
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.