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FDA 510(k)

sam 2.0 长时超声系统

K号: K191568 · 2020-03-06

决定日期2020-03-06
产品代码PFW
咨询委员会PM 请注意,由于您没有提供具体的医疗设备监管文本,我无法进行翻译。请提供具体的文本内容,以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

sam 2.0 Long Duration Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is ZetrOZ Systems, LLC. It received FDA 510(k) clearance on 2020-03-06 under 510(k) number K191568. The device is classified under product code PFW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the sam 2.0 Long Duration Ultrasound System?

sam 2.0 Long Duration Ultrasound System is a medical device that received FDA 510(k) clearance on 2020-03-06. The listed applicant is ZetrOZ Systems, LLC. The 510(k) number is K191568.

When did sam 2.0 Long Duration Ultrasound System receive FDA 510(k) clearance?

sam 2.0 Long Duration Ultrasound System received FDA 510(k) clearance on 2020-03-06, under 510(k) number K191568.

Who is the listed applicant for sam 2.0 Long Duration Ultrasound System?

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

What is the FDA product code for sam 2.0 Long Duration Ultrasound System?

The FDA product code for sam 2.0 Long Duration Ultrasound System is PFW.

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。

列明ZetrOZ Systems, 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:PFW)

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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