Clearance Summary
BMS-2000 MOBILE EEG SYSTEM received FDA 510(k) clearance under submission number K891405, sponsored by Buckman Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1989-08-02.
- Submission: K891405
- Applicant / Sponsor: Buckman Co., Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1855
- Decision date: 1989-08-02
Classification & Regulation
This clearance is catalogued under FDA product code GYE and 21 CFR 882.1855, within the Neurology review panel as a Class II device.