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FDA 510(k)

Dukal SMS 灭菌包装

K号: K233262 · 2024-03-22

申请人Dukal, LLC
决定日期2024-03-22
产品代码FRG
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

Dukal SMS Sterilization Wrap is the device name listed in this FDA 510(k) record. The listed applicant is Dukal, LLC. It received FDA 510(k) clearance on 2024-03-22 under 510(k) number K233262. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Dukal SMS Sterilization Wrap?

Dukal SMS Sterilization Wrap is a medical device that received FDA 510(k) clearance on 2024-03-22. The listed applicant is Dukal, LLC. The 510(k) number is K233262.

When did Dukal SMS Sterilization Wrap receive FDA 510(k) clearance?

Dukal SMS Sterilization Wrap received FDA 510(k) clearance on 2024-03-22, under 510(k) number K233262.

Who is the listed applicant for Dukal SMS Sterilization Wrap?

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

What is the FDA product code for Dukal SMS Sterilization Wrap?

The FDA product code for Dukal SMS Sterilization Wrap is FRG.

相关临床试验

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列明Dukal, 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。

相关器械(代码:FRG)

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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