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FDA 510(k)

空气压缩治疗系统

K号: K192466 · 2020-06-22

决定日期2020-06-22
产品代码IRP
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

Air Compression Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Lifotronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-06-22 under 510(k) number K192466. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Air Compression Therapy System?

Air Compression Therapy System is a medical device that received FDA 510(k) clearance on 2020-06-22. The listed applicant is Shenzhen Lifotronic Technology Co., Ltd.. The 510(k) number is K192466.

When did Air Compression Therapy System receive FDA 510(k) clearance?

Air Compression Therapy System received FDA 510(k) clearance on 2020-06-22, under 510(k) number K192466.

Who is the listed applicant for Air Compression Therapy System?

The FDA 510(k) record lists Shenzhen Lifotronic Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Air Compression Therapy System?

The FDA product code for Air Compression Therapy System is IRP.

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Shenzhen Lifotronic Technology Co., Ltd.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:IRP)

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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