TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026)
K-Number: K250360 · 2025-05-11
Device Summary
Frequently Asked Questions
What is the TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026)?
TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026) is a medical device that received FDA 510(k) clearance on 2025-05-11. It is manufactured by Shenzhen Jiantuo Electronics Co., Ltd.. The 510(k) number is K250360.
When was TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026) approved by the FDA?
TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026) received FDA 510(k) clearance on 2025-05-11, under approval number K250360.
What company makes TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026)?
TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026) is manufactured by Shenzhen Jiantuo Electronics Co., Ltd..
What is the FDA product code for TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026)?
The FDA product code for TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026) is NUH.
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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.