FDA 510(k)

设备名称：BriefCase-Triage：CARE多分级CT身体

K号: K252970 · 2026-01-07

决定日期2026-01-07

产品代码QAS

咨询委员会RA

决定实质等同

器械摘要

BriefCase-Triage: CARE Multi-triage CT Body is the device name listed in this FDA 510(k) record. The listed applicant is Aidoc Medical , Ltd.. It received FDA 510(k) clearance on 2026-01-07 under 510(k) number K252970. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BriefCase-Triage: CARE Multi-triage CT Body?

BriefCase-Triage: CARE Multi-triage CT Body is a medical device that received FDA 510(k) clearance on 2026-01-07. The listed applicant is Aidoc Medical , Ltd.. The 510(k) number is K252970.

When did BriefCase-Triage: CARE Multi-triage CT Body receive FDA 510(k) clearance?

BriefCase-Triage: CARE Multi-triage CT Body received FDA 510(k) clearance on 2026-01-07, under 510(k) number K252970.

Who is the listed applicant for BriefCase-Triage: CARE Multi-triage CT Body?

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

What is the FDA product code for BriefCase-Triage: CARE Multi-triage CT Body?

The FDA product code for BriefCase-Triage: CARE Multi-triage CT Body is QAS.

列明Aidoc Medical , Ltd.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。

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官方来源

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