FDA 510(k)Fist Assist 设备型号 FA-1
K号: K210281 · 2021-06-17
决定日期2021-06-17
产品代码IRP
咨询委员会PM
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决定实质等同
器械摘要
Fist Assist Devices Model FA-1 is the device name listed in this FDA 510(k) record. The listed applicant is Fist Assist Devices, LLC. It received FDA 510(k) clearance on 2021-06-17 under 510(k) number K210281. 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 Fist Assist Devices Model FA-1?
Fist Assist Devices Model FA-1 is a medical device that received FDA 510(k) clearance on 2021-06-17. The listed applicant is Fist Assist Devices, LLC. The 510(k) number is K210281.
When did Fist Assist Devices Model FA-1 receive FDA 510(k) clearance?
Fist Assist Devices Model FA-1 received FDA 510(k) clearance on 2021-06-17, under 510(k) number K210281.
Who is the listed applicant for Fist Assist Devices Model FA-1?
The FDA 510(k) record lists Fist Assist Devices, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fist Assist Devices Model FA-1?
The FDA product code for Fist Assist Devices Model FA-1 is IRP.
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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。
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