Clearance Summary
Medical Imaging Calibration Feature (MICF) received FDA 510(k) clearance under submission number K253582, sponsored by Apple, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-04-01.
- Submission: K253582
- Applicant / Sponsor: Apple, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1940
- Decision date: 2026-04-01
Classification & Regulation
This clearance is catalogued under FDA product code SHN and 21 CFR 892.1940, within the Radiology review panel as a Class I device.