Electronic Muscle Stimulator (Model MP01)— 510(k) K233035
Substantially EquivalentShenzhen Hengbosi Industrial Co., Ltd.
FDA 510(k) clearance K233035 for Electronic Muscle Stimulator (Model MP01), Substantially Equivalent on 2024-01-08. Applicant: Shenzhen Hengbosi Industrial Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Hengbosi Industrial Co., Ltd.
- Product code
- Code NGX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Recent devices under product code NGX
view allData sourced from openFDA. This site is unofficial and independent of the FDA.