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FDA 510(k)

皮肤诊所硝基清疣去除剂

K号: K242932 · 2025-04-15

决定日期2025-04-15
产品代码GEH
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决定实质等同

器械摘要

Skin Clinic Nitro Clear Wart Remover is the device name listed in this FDA 510(k) record. The listed applicant is Cryoconcepts LP. It received FDA 510(k) clearance on 2025-04-15 under 510(k) number K242932. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Skin Clinic Nitro Clear Wart Remover?

Skin Clinic Nitro Clear Wart Remover is a medical device that received FDA 510(k) clearance on 2025-04-15. The listed applicant is Cryoconcepts LP. The 510(k) number is K242932.

When did Skin Clinic Nitro Clear Wart Remover receive FDA 510(k) clearance?

Skin Clinic Nitro Clear Wart Remover received FDA 510(k) clearance on 2025-04-15, under 510(k) number K242932.

Who is the listed applicant for Skin Clinic Nitro Clear Wart Remover?

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

What is the FDA product code for Skin Clinic Nitro Clear Wart Remover?

The FDA product code for Skin Clinic Nitro Clear Wart Remover is GEH.

相关临床试验

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列明Cryoconcepts LP为申报人的其他记录

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相关器械(代码:GEH)

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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