免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

无线探头式超声扫描仪

K号: K252709 · 2026-04-02

决定日期2026-04-02
产品代码IYN
咨询委员会RA
决定实质等同

器械摘要

Wireless Probe Type Ultrasound Scanner is the device name listed in this FDA 510(k) record. The listed applicant is Xuzhou Yongkang Electronic Science Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-04-02 under 510(k) number K252709. 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 Wireless Probe Type Ultrasound Scanner?

Wireless Probe Type Ultrasound Scanner is a medical device that received FDA 510(k) clearance on 2026-04-02. The listed applicant is Xuzhou Yongkang Electronic Science Technology Co., Ltd.. The 510(k) number is K252709.

When did Wireless Probe Type Ultrasound Scanner receive FDA 510(k) clearance?

Wireless Probe Type Ultrasound Scanner received FDA 510(k) clearance on 2026-04-02, under 510(k) number K252709.

Who is the listed applicant for Wireless Probe Type Ultrasound Scanner?

The FDA 510(k) record lists Xuzhou Yongkang Electronic Science Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Wireless Probe Type Ultrasound Scanner?

The FDA product code for Wireless Probe Type Ultrasound Scanner is IYN.

相关临床试验

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。

列明Xuzhou Yongkang Electronic Science Technology 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。

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

在 FDA 数据库中查看 →

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。

↑