K233035
- 510(k) number
- K233035
- Device name
- Electronic Muscle Stimulator (Model MP01)
- Applicant
- Shenzhen Hengbosi Industrial Co., Ltd. CN
- Product code
- NGX — Stimulator, Muscle, Powered, For Muscle Conditioning
- Decision date
- 2024-01-08
- Date received
- 2023-09-25
- 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: K233035
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.