K242787
- 510(k) number
- K242787
- Device name
- Tens & Ems Device (TU1080)
- Applicant
- Changsha Anxiang Medical Technology Co., Ltd. CN
- Product code
- NGX — Stimulator, Muscle, Powered, For Muscle Conditioning
- Decision date
- 2024-12-18
- Date received
- 2024-09-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K242787
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.