Transcutaneous Electrical Nerve Stimulator (K6106)
K-Number: K241119 · 2024-07-22
Device Summary
Frequently Asked Questions
What is the Transcutaneous Electrical Nerve Stimulator (K6106)?
Transcutaneous Electrical Nerve Stimulator (K6106) is a medical device that received FDA 510(k) clearance on 2024-07-22. It is manufactured by Shenzhen Yicai Health Technology Co., Ltd.. The 510(k) number is K241119.
When was Transcutaneous Electrical Nerve Stimulator (K6106) approved by the FDA?
Transcutaneous Electrical Nerve Stimulator (K6106) received FDA 510(k) clearance on 2024-07-22, under approval number K241119.
What company makes Transcutaneous Electrical Nerve Stimulator (K6106)?
Transcutaneous Electrical Nerve Stimulator (K6106) is manufactured by Shenzhen Yicai Health Technology Co., Ltd..
What is the FDA product code for Transcutaneous Electrical Nerve Stimulator (K6106)?
The FDA product code for Transcutaneous Electrical Nerve Stimulator (K6106) is NUH.
Related Clinical Trials
Related PubMed Literature
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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.