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FDA 510(k)

Optiflow 氧气套件

K号: K211096 · 2022-01-28

决定日期2022-01-28
产品代码BTT
咨询委员会AN 请注意,由于您没有提供完整的医疗设备监管文本,我无法提供完整的翻译。如果您能提供完整的文本,我将很乐意为您翻译。
决定实质等同

器械摘要

Optiflow Oxygen Kit is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Healthcare, Ltd.. It received FDA 510(k) clearance on 2022-01-28 under 510(k) number K211096. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Optiflow Oxygen Kit?

Optiflow Oxygen Kit is a medical device that received FDA 510(k) clearance on 2022-01-28. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K211096.

When did Optiflow Oxygen Kit receive FDA 510(k) clearance?

Optiflow Oxygen Kit received FDA 510(k) clearance on 2022-01-28, under 510(k) number K211096.

Who is the listed applicant for Optiflow Oxygen Kit?

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

What is the FDA product code for Optiflow Oxygen Kit?

The FDA product code for Optiflow Oxygen Kit is BTT.

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列明Fisher & Paykel Healthcare, Ltd.为申报人的其他记录

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相关器械(代码:BTT)

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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