FDA 510(k)

数字超声诊断成像系统（型号：F6）

K号: K231930 · 2024-03-22

决定日期2024-03-22

产品代码IYN

咨询委员会RA

决定实质等同

器械摘要

Digital Ultrasonic Diagnostic Imaging System (Model: F6) is the device name listed in this FDA 510(k) record. The listed applicant is Guangdong Youkey Medical Co., Ltd.. It received FDA 510(k) clearance on 2024-03-22 under 510(k) number K231930. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Digital Ultrasonic Diagnostic Imaging System (Model: F6)?

Digital Ultrasonic Diagnostic Imaging System (Model: F6) is a medical device that received FDA 510(k) clearance on 2024-03-22. The listed applicant is Guangdong Youkey Medical Co., Ltd.. The 510(k) number is K231930.

When did Digital Ultrasonic Diagnostic Imaging System (Model: F6) receive FDA 510(k) clearance?

Digital Ultrasonic Diagnostic Imaging System (Model: F6) received FDA 510(k) clearance on 2024-03-22, under 510(k) number K231930.

Who is the listed applicant for Digital Ultrasonic Diagnostic Imaging System (Model: F6)?

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

What is the FDA product code for Digital Ultrasonic Diagnostic Imaging System (Model: F6)?

The FDA product code for Digital Ultrasonic Diagnostic Imaging System (Model: F6) is IYN.

列明Guangdong Youkey Medical Co., 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。

K211746口袋超声系统

相关器械（代码：IYN）

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。

官方来源

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