TENS & EMS Device— 510(k) K213835

Substantially Equivalent

Shenzhen Jian Feng Electronic Technology Co., Ltd.

FDA 510(k) clearance K213835 for TENS & EMS Device, Substantially Equivalent on 2022-03-03. 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: 2021-12-09
Decision date: 2022-03-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.