FDA 510(k)

Interson USB超声系统

K号: K233734 · 2023-12-22

决定日期2023-12-22

产品代码IYN

咨询委员会RA

决定实质等同

器械摘要

Interson USB Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Interson Corporation. It received FDA 510(k) clearance on 2023-12-22 under 510(k) number K233734. 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 Interson USB Ultrasound System?

Interson USB Ultrasound System is a medical device that received FDA 510(k) clearance on 2023-12-22. The listed applicant is Interson Corporation. The 510(k) number is K233734.

When did Interson USB Ultrasound System receive FDA 510(k) clearance?

Interson USB Ultrasound System received FDA 510(k) clearance on 2023-12-22, under 510(k) number K233734.

Who is the listed applicant for Interson USB Ultrasound System?

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

What is the FDA product code for Interson USB Ultrasound System?

The FDA product code for Interson USB Ultrasound System is IYN.

列明Interson Corporation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。

K163443Interson USB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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