Clearance Summary
NUAMPS received FDA 510(k) clearance under submission number K023536, sponsored by Neuroscan. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2003-01-15.
- Submission: K023536
- Applicant / Sponsor: Neuroscan
- Clearance pathway: Abbreviated
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1400
- Decision date: 2003-01-15
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.