TENS & EMS Device
K-Number: K213835 · 2022-03-03
Decision Date2022-03-03
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
TENS & EMS Device is a medical device manufactured by Shenzhen Jian Feng Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-03-03 under approval number K213835. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TENS & EMS Device?
TENS & EMS Device is a medical device that received FDA 510(k) clearance on 2022-03-03. It is manufactured by Shenzhen Jian Feng Electronic Technology Co., Ltd.. The 510(k) number is K213835.
When was TENS & EMS Device approved by the FDA?
TENS & EMS Device received FDA 510(k) clearance on 2022-03-03, under approval number K213835.
What company makes TENS & EMS Device?
TENS & EMS Device is manufactured by Shenzhen Jian Feng Electronic Technology Co., Ltd..
What is the FDA product code for TENS & EMS Device?
The FDA product code for TENS & EMS Device is NUH.
Other Devices by Shenzhen Jian Feng Electronic Technology Co., Ltd.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.