Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Digital Prism Correction Feature (DPCF)

K-Number: K250143 · 2025-06-23

ApplicantApple, Inc.
Decision Date2025-06-23
Product CodeSCW
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Digital Prism Correction Feature (DPCF) is the device name listed in this FDA 510(k) record. The listed applicant is Apple, Inc.. It received FDA 510(k) clearance on 2025-06-23 under 510(k) number K250143. The device is classified under product code SCW. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Digital Prism Correction Feature (DPCF)?

Digital Prism Correction Feature (DPCF) is a medical device that received FDA 510(k) clearance on 2025-06-23. The listed applicant is Apple, Inc.. The 510(k) number is K250143.

When did Digital Prism Correction Feature (DPCF) receive FDA 510(k) clearance?

Digital Prism Correction Feature (DPCF) received FDA 510(k) clearance on 2025-06-23, under 510(k) number K250143.

Who is the listed applicant for Digital Prism Correction Feature (DPCF)?

The FDA 510(k) record lists Apple, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Digital Prism Correction Feature (DPCF)?

The FDA product code for Digital Prism Correction Feature (DPCF) is SCW.

Other records listing Apple, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253582Medical Imaging Calibration Feature (MICF)K250507Hypertension Notification Feature (HTNF)K242058Digital Prism Correction Feature (DPCF)K240929Sleep Apnea Notification Feature (SANF)K231173Irregular Rhythm Notification Feature (IRNF)K213971Atrial Fibrillation History Feature

View all 9 devices →

Related Devices (Code: SCW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242058Digital Prism Correction Feature (DPCF)Apple, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑