FDA 510(k)

Silverlon® 伤口接触，烧伤接触敷料

K号: K241225 · 2024-07-31

决定日期2024-07-31

产品代码FRO

决定实质等同

器械摘要

Silverlon® Wound Contact, Burn Contact Dressing is the device name listed in this FDA 510(k) record. The listed applicant is Argentum Medical, LLC. It received FDA 510(k) clearance on 2024-07-31 under 510(k) number K241225. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常见问题

What is the Silverlon® Wound Contact, Burn Contact Dressing?

Silverlon® Wound Contact, Burn Contact Dressing is a medical device that received FDA 510(k) clearance on 2024-07-31. The listed applicant is Argentum Medical, LLC. The 510(k) number is K241225.

When did Silverlon® Wound Contact, Burn Contact Dressing receive FDA 510(k) clearance?

Silverlon® Wound Contact, Burn Contact Dressing received FDA 510(k) clearance on 2024-07-31, under 510(k) number K241225.

Who is the listed applicant for Silverlon® Wound Contact, Burn Contact Dressing?

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

What is the FDA product code for Silverlon® Wound Contact, Burn Contact Dressing?

The FDA product code for Silverlon® Wound Contact, Burn Contact Dressing is FRO. This falls under the Anesthesiology category.

列明Argentum Medical, LLC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。

K190343Silverlon 伤口接触，烧伤接触敷料 K180570Silverlon 岛屿伤口敷料，Silverlon 伤口垫敷料（也称为 Silverlon 烧伤垫敷料）

官方来源

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