Aurora-RT
K号: K213526 · 2022-05-04
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器械摘要
Aurora-RT is the device name listed in this FDA 510(k) record. The listed applicant is Magnettx Oncology Solutions , Ltd.. It received FDA 510(k) clearance on 2022-05-04 under 510(k) number K213526. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Aurora-RT?
Aurora-RT is a medical device that received FDA 510(k) clearance on 2022-05-04. The listed applicant is Magnettx Oncology Solutions , Ltd.. The 510(k) number is K213526.
When did Aurora-RT receive FDA 510(k) clearance?
Aurora-RT received FDA 510(k) clearance on 2022-05-04, under 510(k) number K213526.
Who is the listed applicant for Aurora-RT?
The FDA 510(k) record lists Magnettx Oncology Solutions , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aurora-RT?
The FDA product code for Aurora-RT is IYE.
相关临床试验
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相关器械（代码：IYE）
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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