FDA 510(k)

Sapphire 套件

K号: K171346 · 2017-08-25

决定日期2017-08-25

产品代码MRZ

咨询委员会医疗设备监管文本翻译如下： HO 请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。

决定实质等同

器械摘要

Sapphire Sets is the device name listed in this FDA 510(k) record. The listed applicant is Icu Medical. It received FDA 510(k) clearance on 2017-08-25 under 510(k) number K171346. The device is classified under product code MRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sapphire Sets?

Sapphire Sets is a medical device that received FDA 510(k) clearance on 2017-08-25. The listed applicant is Icu Medical. The 510(k) number is K171346.

When did Sapphire Sets receive FDA 510(k) clearance?

Sapphire Sets received FDA 510(k) clearance on 2017-08-25, under 510(k) number K171346.

Who is the listed applicant for Sapphire Sets?

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

What is the FDA product code for Sapphire Sets?

The FDA product code for Sapphire Sets is MRZ.

列明Icu Medical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。

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