Stryker 面部識別系統
K 號：K232350 · 2024-01-13
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器材摘要
Stryker Facial iD System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Craniomaxillofacial. It received FDA 510(k) clearance on 2024-01-13 under 510(k) number K232350. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Stryker Facial iD System?
Stryker Facial iD System is a medical device that received FDA 510(k) clearance on 2024-01-13. The listed applicant is Stryker Craniomaxillofacial. The 510(k) number is K232350.
When did Stryker Facial iD System receive FDA 510(k) clearance?
Stryker Facial iD System received FDA 510(k) clearance on 2024-01-13, under 510(k) number K232350.
Who is the listed applicant for Stryker Facial iD System?
The FDA 510(k) record lists Stryker Craniomaxillofacial as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stryker Facial iD System?
The FDA product code for Stryker Facial iD System is JEY.
相關臨床試驗
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相關器械（代碼：JEY）
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。
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官方來源
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