FDA 510(k)

彩虹粘贴染色剂 SE

K号: K233885 · 2024-06-21

决定日期2024-06-21

产品代码EIH

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决定实质等同

器械摘要

rainbow Paste Stain SE is the device name listed in this FDA 510(k) record. The listed applicant is Genoss Co., Ltd.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233885. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the rainbow Paste Stain SE?

rainbow Paste Stain SE is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Genoss Co., Ltd.. The 510(k) number is K233885.

When did rainbow Paste Stain SE receive FDA 510(k) clearance?

rainbow Paste Stain SE received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233885.

Who is the listed applicant for rainbow Paste Stain SE?

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

What is the FDA product code for rainbow Paste Stain SE?

The FDA product code for rainbow Paste Stain SE is EIH.

列明Genoss Co., Ltd.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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官方来源

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