Clearance Summary
STACKED ABR FOR NAVIGATOR PRO received FDA 510(k) clearance under submission number K030907, sponsored by Bio-Logic Systems Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2003-05-09.
- Submission: K030907
- Applicant / Sponsor: Bio-Logic Systems Corp.
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1900
- Decision date: 2003-05-09
Classification & Regulation
This clearance is catalogued under FDA product code GWJ and 21 CFR 882.1900, within the Neurology review panel as a Class II device.