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FDA 510(k)

HydroPearl 微球

K号: K192684 · 2020-01-22

决定日期2020-01-22
产品代码NOY
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定实质等同

器械摘要

HydroPearl Microspheres is the device name listed in this FDA 510(k) record. The listed applicant is MicroVention, Inc.. It received FDA 510(k) clearance on 2020-01-22 under 510(k) number K192684. The device is classified under product code NOY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the HydroPearl Microspheres?

HydroPearl Microspheres is a medical device that received FDA 510(k) clearance on 2020-01-22. The listed applicant is MicroVention, Inc.. The 510(k) number is K192684.

When did HydroPearl Microspheres receive FDA 510(k) clearance?

HydroPearl Microspheres received FDA 510(k) clearance on 2020-01-22, under 510(k) number K192684.

Who is the listed applicant for HydroPearl Microspheres?

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

What is the FDA product code for HydroPearl Microspheres?

The FDA product code for HydroPearl Microspheres is NOY.

相关临床试验

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列明MicroVention, Inc.为申报人的其他记录

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相关器械(代码:NOY)

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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