TENS & EMS DEVICE (Model: FM-B2403A)— 510(k) K213741
Substantially EquivalentShenzhen Jian Feng Electronic Technology Co., Ltd.
FDA 510(k) clearance K213741 for TENS & EMS DEVICE (Model: FM-B2403A), Substantially Equivalent on 2022-03-08. Applicant: Shenzhen Jian Feng Electronic Technology Co., Ltd..
Clearance details
- Applicant
- Shenzhen Jian Feng Electronic Technology Co., Ltd.
- Product code
- Code NUH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.