ETD系列电疗设备
K号: K201958 · 2020-08-04
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决定日期2020-08-04
产品代码IPF
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
ETD Family of Electrotherapy Devices is the device name listed in this FDA 510(k) record. The listed applicant is Therasigma, LLC. It received FDA 510(k) clearance on 2020-08-04 under 510(k) number K201958. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ETD Family of Electrotherapy Devices?
ETD Family of Electrotherapy Devices is a medical device that received FDA 510(k) clearance on 2020-08-04. The listed applicant is Therasigma, LLC. The 510(k) number is K201958.
When did ETD Family of Electrotherapy Devices receive FDA 510(k) clearance?
ETD Family of Electrotherapy Devices received FDA 510(k) clearance on 2020-08-04, under 510(k) number K201958.
Who is the listed applicant for ETD Family of Electrotherapy Devices?
The FDA 510(k) record lists Therasigma, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ETD Family of Electrotherapy Devices?
The FDA product code for ETD Family of Electrotherapy Devices is IPF.
相关临床试验
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列明Therasigma, 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：IPF）
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
在 FDA 数据库中查看 →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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