Clearance Summary
AT235 received FDA 510(k) clearance under submission number K151616, sponsored by Interacoustics A/S. The device was reviewed via the Special premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2015-07-15.
- Submission: K151616
- Applicant / Sponsor: Interacoustics A/S
- Clearance pathway: Special
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1090
- Decision date: 2015-07-15
Classification & Regulation
This clearance is catalogued under FDA product code ETY and 21 CFR 874.1090, within the Ear, Nose, Throat review panel as a Class II device.