Clearance Summary
E-EEGX, N-EEGX received FDA 510(k) clearance under submission number K191322, sponsored by GE Healthcare Finland Oy. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2020-01-22.
- Submission: K191322
- Applicant / Sponsor: GE Healthcare Finland Oy
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1400
- Decision date: 2020-01-22
Classification & Regulation
This clearance is catalogued under FDA product code OLT and 21 CFR 882.1400, within the Neurology review panel as a Class II device.