FDA 510(k)

JJ 系列容器系统

K号: K192056 · 2020-03-27

决定日期2020-03-27

产品代码KCT

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

JJ Series Container System is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2020-03-27 under 510(k) number K192056. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the JJ Series Container System?

JJ Series Container System is a medical device that received FDA 510(k) clearance on 2020-03-27. The listed applicant is Aesculap, Inc.. The 510(k) number is K192056.

When did JJ Series Container System receive FDA 510(k) clearance?

JJ Series Container System received FDA 510(k) clearance on 2020-03-27, under 510(k) number K192056.

Who is the listed applicant for JJ Series Container System?

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

What is the FDA product code for JJ Series Container System?

The FDA product code for JJ Series Container System is KCT.

列明Aesculap, Inc.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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数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。