Perseus
K 號：K192653 · 2020-09-09
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器材摘要
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.
常見問題
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.
相關臨床試驗
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相關器械（代碼：OLO）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
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