FDA 510(k)

Armis VeriCyn 创面冲洗

K号: K220759 · 2023-05-25

决定日期2023-05-25

产品代码FQH

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

Armis VeriCyn Wound Wash is the device name listed in this FDA 510(k) record. The listed applicant is Armis Biopharma, Inc.. It received FDA 510(k) clearance on 2023-05-25 under 510(k) number K220759. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Armis VeriCyn Wound Wash?

Armis VeriCyn Wound Wash is a medical device that received FDA 510(k) clearance on 2023-05-25. The listed applicant is Armis Biopharma, Inc.. The 510(k) number is K220759.

When did Armis VeriCyn Wound Wash receive FDA 510(k) clearance?

Armis VeriCyn Wound Wash received FDA 510(k) clearance on 2023-05-25, under 510(k) number K220759.

Who is the listed applicant for Armis VeriCyn Wound Wash?

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

What is the FDA product code for Armis VeriCyn Wound Wash?

The FDA product code for Armis VeriCyn Wound Wash is FQH.

列明Armis Biopharma, Inc.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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