K252154
- 510(k) number
- K252154
- Device name
- Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)
- Applicant
- Guangzhou Longest Medical Technology Co., Ltd. CN
- Product code
- NGX — Stimulator, Muscle, Powered, For Muscle Conditioning
- Decision date
- 2025-12-09
- Date received
- 2025-07-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K252154.pdf
Official FDA record: K252154
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.