FDA 510(k)

AMSCO 600 蒸汽灭菌器

K号: K232485 · 2023-09-13

申请人Steris

决定日期2023-09-13

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

AMSCO 600 Steam Sterilizer is the device name listed in this FDA 510(k) record. The listed applicant is Steris. It received FDA 510(k) clearance on 2023-09-13 under 510(k) number K232485. 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 AMSCO 600 Steam Sterilizer?

AMSCO 600 Steam Sterilizer is a medical device that received FDA 510(k) clearance on 2023-09-13. The listed applicant is Steris. The 510(k) number is K232485.

When did AMSCO 600 Steam Sterilizer receive FDA 510(k) clearance?

AMSCO 600 Steam Sterilizer received FDA 510(k) clearance on 2023-09-13, under 510(k) number K232485.

Who is the listed applicant for AMSCO 600 Steam Sterilizer?

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

What is the FDA product code for AMSCO 600 Steam Sterilizer?

The FDA product code for AMSCO 600 Steam Sterilizer is FLE.

列明Steris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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