FDA 510(k)Normatec Go
K号: K221666 · 2022-07-14
决定日期2022-07-14
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
Normatec Go is the device name listed in this FDA 510(k) record. The listed applicant is NormaTec Industries, LP. It received FDA 510(k) clearance on 2022-07-14 under 510(k) number K221666. 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 Normatec Go?
Normatec Go is a medical device that received FDA 510(k) clearance on 2022-07-14. The listed applicant is NormaTec Industries, LP. The 510(k) number is K221666.
When did Normatec Go receive FDA 510(k) clearance?
Normatec Go received FDA 510(k) clearance on 2022-07-14, under 510(k) number K221666.
Who is the listed applicant for Normatec Go?
The FDA 510(k) record lists NormaTec Industries, LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Normatec Go?
The FDA product code for Normatec Go is IRP.
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列明NormaTec Industries, LP为申报人的其他记录
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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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