Clearance Summary
INTERACOUSTICS ASSR, ECLIPSE SYSTEM (CABINET NAME) received FDA 510(k) clearance under submission number K070696, 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 2007-06-29.
- Submission: K070696
- Applicant / Sponsor: Interacoustics A/S
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1900
- Decision date: 2007-06-29
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.