Clearance Summary
NEAT 001 received FDA 510(k) clearance under submission number K250058, sponsored by Brain Electrophysiology Laboratory Company, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2025-04-10.
- Submission: K250058
- Applicant / Sponsor: Brain Electrophysiology Laboratory Company, LLC
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1400
- Decision date: 2025-04-10
Classification & Regulation
This clearance is catalogued under FDA product code OLZ and 21 CFR 882.1400, within the Neurology review panel as a Class II device.