Perseus
K号: K192653 · 2020-09-09
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决定日期2020-09-09
产品代码OLO
咨询委员会NE
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决定实质等同
器械摘要
Perseus is the device name listed in this FDA 510(k) record. The listed applicant is Orthokey Italia S.R.L.. It received FDA 510(k) clearance on 2020-09-09 under 510(k) number K192653. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Perseus?
Perseus is a medical device that received FDA 510(k) clearance on 2020-09-09. The listed applicant is Orthokey Italia S.R.L.. The 510(k) number is K192653.
When did Perseus receive FDA 510(k) clearance?
Perseus received FDA 510(k) clearance on 2020-09-09, under 510(k) number K192653.
Who is the listed applicant for Perseus?
The FDA 510(k) record lists Orthokey Italia S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Perseus?
The FDA product code for Perseus is OLO.
相关临床试验
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相关器械（代码：OLO）
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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