Clearance Summary
DYNAMIC NEUROSCREENING DEVICE received FDA 510(k) clearance under submission number K141208, sponsored by Prosenex. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2014-07-23.
- Submission: K141208
- Applicant / Sponsor: Prosenex
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class I
- Regulation citation: 21 CFR 882.1200
- Decision date: 2014-07-23
Classification & Regulation
This clearance is catalogued under FDA product code LQW and 21 CFR 882.1200, within the Neurology review panel as a Class I device.