Clearance Summary
SPECTRAL EEG MONITOR MODEL B500 received FDA 510(k) clearance under submission number K913051, sponsored by Biometrak Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1991-08-20.
- Submission: K913051
- Applicant / Sponsor: Biometrak Corp.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1400
- Decision date: 1991-08-20
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.