Clearance Summary
Digital Prism Correction Feature (DPCF) received FDA 510(k) clearance under submission number K250143, sponsored by Apple, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2025-06-23.
- Submission: K250143
- Applicant / Sponsor: Apple, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1655
- Decision date: 2025-06-23
Classification & Regulation
This clearance is catalogued under FDA product code SCW and 21 CFR 886.1655, within the Ophthalmic review panel as a Class I device.