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FDA 510(k)

蒸汽灭菌器 B17 B22 系列系列

K号: K161848 · 2017-02-23

申请人Cefla S.C.
决定日期2017-02-23
产品代码FLE
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

Family of Steam sterilizers B17 B22 Series is the device name listed in this FDA 510(k) record. The listed applicant is Cefla S.C.. It received FDA 510(k) clearance on 2017-02-23 under 510(k) number K161848. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Family of Steam sterilizers B17 B22 Series?

Family of Steam sterilizers B17 B22 Series is a medical device that received FDA 510(k) clearance on 2017-02-23. The listed applicant is Cefla S.C.. The 510(k) number is K161848.

When did Family of Steam sterilizers B17 B22 Series receive FDA 510(k) clearance?

Family of Steam sterilizers B17 B22 Series received FDA 510(k) clearance on 2017-02-23, under 510(k) number K161848.

Who is the listed applicant for Family of Steam sterilizers B17 B22 Series?

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

What is the FDA product code for Family of Steam sterilizers B17 B22 Series?

The FDA product code for Family of Steam sterilizers B17 B22 Series is FLE.

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列明Cefla S.C.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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相关器械(代码:FLE)

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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