Clearance Summary
Disposable Non-invasive EEG Sensor received FDA 510(k) clearance under submission number K220448, sponsored by Shenzhen Med-Link Electronics Tech Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2023-01-19.
- Submission: K220448
- Applicant / Sponsor: Shenzhen Med-Link Electronics Tech Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1320
- Decision date: 2023-01-19
Classification & Regulation
This clearance is catalogued under FDA product code GXY and 21 CFR 882.1320, within the Neurology review panel as a Class II device.