Clearance Summary
Iridex 810 Laser received FDA 510(k) clearance under submission number K202760, sponsored by Iridex Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2020-10-21.
- Submission: K202760
- Applicant / Sponsor: Iridex Corporation
- Clearance pathway: Special
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4390
- Decision date: 2020-10-21
Classification & Regulation
This clearance is catalogued under FDA product code HQF and 21 CFR 886.4390, within the Ophthalmic review panel as a Class II device.