Clearance Summary
EYESEECAM VHIT received FDA 510(k) clearance under submission number K131681, sponsored by Interacoustics A/S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2013-09-06.
- Submission: K131681
- Applicant / Sponsor: Interacoustics A/S
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1460
- Decision date: 2013-09-06
Classification & Regulation
This clearance is catalogued under FDA product code GWN and 21 CFR 882.1460, within the Neurology review panel as a Class II device.