SECURE-LOCK
K 號：K220906 · 2022-07-22
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器材摘要
SECURE-LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Xiros, Ltd.. It received FDA 510(k) clearance on 2022-07-22 under 510(k) number K220906. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the SECURE-LOCK?
SECURE-LOCK is a medical device that received FDA 510(k) clearance on 2022-07-22. The listed applicant is Xiros, Ltd.. The 510(k) number is K220906.
When did SECURE-LOCK receive FDA 510(k) clearance?
SECURE-LOCK received FDA 510(k) clearance on 2022-07-22, under 510(k) number K220906.
Who is the listed applicant for SECURE-LOCK?
The FDA 510(k) record lists Xiros, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SECURE-LOCK?
The FDA product code for SECURE-LOCK is HTY.
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其他以 Xiros, Ltd. 為申請人之記錄
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。
相關器械（代碼：HTY）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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