FDA 510(k)

数字棱镜校正功能（DPCF）

K号: K250143 · 2025-06-23

决定日期2025-06-23

产品代码SCW

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决定实质等同

器械摘要

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.

常见问题

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.

列明Apple, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K253582医疗成像校准功能（MICF）K250507高血压通知功能（HTNF）K242058数字棱镜校正功能（DPCF）K240929睡眠呼吸暂停通知功能（SANF）K231173心律不齐通知功能（IRNF）K213971房颤病史功能

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官方来源

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