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FDA 510(k)

Dolphin/IQ 和 Dolphin/4D

K号: K170859 · 2017-11-14

决定日期2017-11-14
产品代码IYN
咨询委员会RA
决定实质等同

器械摘要

Dolphin/IQ and Dolphin/4D is the device name listed in this FDA 510(k) record. The listed applicant is Viasonix , Ltd.. It received FDA 510(k) clearance on 2017-11-14 under 510(k) number K170859. 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 Dolphin/IQ and Dolphin/4D?

Dolphin/IQ and Dolphin/4D is a medical device that received FDA 510(k) clearance on 2017-11-14. The listed applicant is Viasonix , Ltd.. The 510(k) number is K170859.

When did Dolphin/IQ and Dolphin/4D receive FDA 510(k) clearance?

Dolphin/IQ and Dolphin/4D received FDA 510(k) clearance on 2017-11-14, under 510(k) number K170859.

Who is the listed applicant for Dolphin/IQ and Dolphin/4D?

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

What is the FDA product code for Dolphin/IQ and Dolphin/4D?

The FDA product code for Dolphin/IQ and Dolphin/4D 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Viasonix , Ltd.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。

官方来源

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