Clearance Summary
AAIO-7, AAIO WIRLESS received FDA 510(k) clearance under submission number K110205, sponsored by Appasamy Associates. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2011-02-09.
- Submission: K110205
- Applicant / Sponsor: Appasamy Associates
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1570
- Decision date: 2011-02-09
Classification & Regulation
This clearance is catalogued under FDA product code HLI and 21 CFR 886.1570, within the Ophthalmic review panel as a Class II device.