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FDA 510(k)

超声波网状雾化器

K号: K201397 · 2021-06-14

决定日期2021-06-14
产品代码CAF
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

Ultrasonic Mesh Nebulizer is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Ivankaca Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-06-14 under 510(k) number K201397. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Ultrasonic Mesh Nebulizer?

Ultrasonic Mesh Nebulizer is a medical device that received FDA 510(k) clearance on 2021-06-14. The listed applicant is Shenzhen Ivankaca Technology Co., Ltd.. The 510(k) number is K201397.

When did Ultrasonic Mesh Nebulizer receive FDA 510(k) clearance?

Ultrasonic Mesh Nebulizer received FDA 510(k) clearance on 2021-06-14, under 510(k) number K201397.

Who is the listed applicant for Ultrasonic Mesh Nebulizer?

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

What is the FDA product code for Ultrasonic Mesh Nebulizer?

The FDA product code for Ultrasonic Mesh Nebulizer is CAF.

相关临床试验

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相关器械(代码:CAF)

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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