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FDA 510(k)

Aixplorer & Aixplorer Ultimate超声诊断系统

K号: K173021 · 2018-01-09

决定日期2018-01-09
产品代码IYN
咨询委员会RA
决定实质等同

器械摘要

Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems is the device name listed in this FDA 510(k) record. The listed applicant is Supersonic Imagine. It received FDA 510(k) clearance on 2018-01-09 under 510(k) number K173021. 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 Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems?

Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems is a medical device that received FDA 510(k) clearance on 2018-01-09. The listed applicant is Supersonic Imagine. The 510(k) number is K173021.

When did Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems receive FDA 510(k) clearance?

Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems received FDA 510(k) clearance on 2018-01-09, under 510(k) number K173021.

Who is the listed applicant for Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems?

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

What is the FDA product code for Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems?

The FDA product code for Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems is IYN.

相关临床试验

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列明Supersonic Imagine为申报人的其他记录

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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。

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