BeamSite
K号: K200940 · 2020-12-11
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器械摘要
BeamSite is the device name listed in this FDA 510(k) record. The listed applicant is Doseoptics, LLC. It received FDA 510(k) clearance on 2020-12-11 under 510(k) number K200940. 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 BeamSite?
BeamSite is a medical device that received FDA 510(k) clearance on 2020-12-11. The listed applicant is Doseoptics, LLC. The 510(k) number is K200940.
When did BeamSite receive FDA 510(k) clearance?
BeamSite received FDA 510(k) clearance on 2020-12-11, under 510(k) number K200940.
Who is the listed applicant for BeamSite?
The FDA 510(k) record lists Doseoptics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BeamSite?
The FDA product code for BeamSite is IYE.
相关临床试验
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列明Doseoptics, LLC为申报人的其他记录
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。
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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