Clearance Summary
VISUREF 600 received FDA 510(k) clearance under submission number K253834, sponsored by Carl Zeiss Vision GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2026-03-18.
- Submission: K253834
- Applicant / Sponsor: Carl Zeiss Vision GmbH
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1850
- Decision date: 2026-03-18
Classification & Regulation
This clearance is catalogued under FDA product code HJO and 21 CFR 886.1850, within the Ophthalmic review panel as a Class II device.