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FDA 510(k)

gke 斯特里-记录蒸汽迷你生物-生物+自包含生物指示剂(SCBI)

K号: K163144 · 2017-04-07

申请人Gke-GmbH
决定日期2017-04-07
产品代码FRC
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

gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI) is the device name listed in this FDA 510(k) record. The listed applicant is Gke-GmbH. It received FDA 510(k) clearance on 2017-04-07 under 510(k) number K163144. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI)?

gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI) is a medical device that received FDA 510(k) clearance on 2017-04-07. The listed applicant is Gke-GmbH. The 510(k) number is K163144.

When did gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI) receive FDA 510(k) clearance?

gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI) received FDA 510(k) clearance on 2017-04-07, under 510(k) number K163144.

Who is the listed applicant for gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI)?

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

What is the FDA product code for gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI)?

The FDA product code for gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI) is FRC.

相关临床试验

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:FRC)

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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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。

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