FDA 510(k)

Bunkerhill 腹主动脉量化 (AAQ)

K号: K243779 · 2025-07-01

决定日期2025-07-01

产品代码QIH

咨询委员会RA

决定实质等同

器械摘要

Bunkerhill Abdominal Aortic Quantification (AAQ) is the device name listed in this FDA 510(k) record. The listed applicant is BunkerHill Health. It received FDA 510(k) clearance on 2025-07-01 under 510(k) number K243779. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Bunkerhill Abdominal Aortic Quantification (AAQ)?

Bunkerhill Abdominal Aortic Quantification (AAQ) is a medical device that received FDA 510(k) clearance on 2025-07-01. The listed applicant is BunkerHill Health. The 510(k) number is K243779.

When did Bunkerhill Abdominal Aortic Quantification (AAQ) receive FDA 510(k) clearance?

Bunkerhill Abdominal Aortic Quantification (AAQ) received FDA 510(k) clearance on 2025-07-01, under 510(k) number K243779.

Who is the listed applicant for Bunkerhill Abdominal Aortic Quantification (AAQ)?

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

What is the FDA product code for Bunkerhill Abdominal Aortic Quantification (AAQ)?

The FDA product code for Bunkerhill Abdominal Aortic Quantification (AAQ) is QIH.

列明BunkerHill Health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。

K260167Bunkerhill 对比 AVC K260166Bunkerhill 对比 CAC K250662Bunkerhill MAC K250649Bunkerhill ECG-EF K242295BunkerHill BMD K243229Bunkerhill AVC

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官方来源

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数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。