ParaMotion
K号: K203761 · 2022-01-21
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决定日期2022-01-21
产品代码IPL
咨询委员会PM
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决定实质等同
器械摘要
ParaMotion is the device name listed in this FDA 510(k) record. The listed applicant is Powerbasetec GmbH. It received FDA 510(k) clearance on 2022-01-21 under 510(k) number K203761. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ParaMotion?
ParaMotion is a medical device that received FDA 510(k) clearance on 2022-01-21. The listed applicant is Powerbasetec GmbH. The 510(k) number is K203761.
When did ParaMotion receive FDA 510(k) clearance?
ParaMotion received FDA 510(k) clearance on 2022-01-21, under 510(k) number K203761.
Who is the listed applicant for ParaMotion?
The FDA 510(k) record lists Powerbasetec GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ParaMotion?
The FDA product code for ParaMotion is IPL.
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相关器械（代码：IPL）
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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官方来源
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