FDA 510(k)Xrecovery(XR-001)
K号: K242940 · 2024-11-14
决定日期2024-11-14
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
Xrecovery (XR-001) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Xinrun Electric Appliances Co, Ltd.. It received FDA 510(k) clearance on 2024-11-14 under 510(k) number K242940. 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 Xrecovery (XR-001)?
Xrecovery (XR-001) is a medical device that received FDA 510(k) clearance on 2024-11-14. The listed applicant is Shenzhen Xinrun Electric Appliances Co, Ltd.. The 510(k) number is K242940.
When did Xrecovery (XR-001) receive FDA 510(k) clearance?
Xrecovery (XR-001) received FDA 510(k) clearance on 2024-11-14, under 510(k) number K242940.
Who is the listed applicant for Xrecovery (XR-001)?
The FDA 510(k) record lists Shenzhen Xinrun Electric Appliances Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Xrecovery (XR-001)?
The FDA product code for Xrecovery (XR-001) 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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