Cypris eXact 緝合定位設備
K 號：K240185 · 2024-05-03
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器材摘要
Cypris eXact Suture Placement Device is the device name listed in this FDA 510(k) record. The listed applicant is Cypris Medical. It received FDA 510(k) clearance on 2024-05-03 under 510(k) number K240185. The device is classified under product code GEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Cypris eXact Suture Placement Device?
Cypris eXact Suture Placement Device is a medical device that received FDA 510(k) clearance on 2024-05-03. The listed applicant is Cypris Medical. The 510(k) number is K240185.
When did Cypris eXact Suture Placement Device receive FDA 510(k) clearance?
Cypris eXact Suture Placement Device received FDA 510(k) clearance on 2024-05-03, under 510(k) number K240185.
Who is the listed applicant for Cypris eXact Suture Placement Device?
The FDA 510(k) record lists Cypris Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cypris eXact Suture Placement Device?
The FDA product code for Cypris eXact Suture Placement Device is GEJ.
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其他以 Cypris Medical 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。
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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