組織膠粘劑，內用
PMA 核准號：P130023 · 2017-07-27
廣告
決定日期2017-07-27
PMA 編號P130023
產品代碼PJK
器械分類3 類
醫療專科G
法規編號21 CFR 8
諮詢委員會SU
請提供完整的描述文本，以便我進行翻譯。
器材摘要
Tissue adhesive for internal use is the device name listed in this FDA 510(k) record. The listed applicant is Cohera Medical, Inc.. It received FDA 510(k) clearance on 2017-07-27. The device is classified under product code PJK. It was reviewed by the SU advisory panel.
常見問題
What is the Tissue adhesive for internal use?
Tissue adhesive for internal use is a medical device that received FDA 510(k) clearance on 2017-07-27. The listed applicant is Cohera Medical, Inc..
When did Tissue adhesive for internal use receive FDA 510(k) clearance?
The clearance date for Tissue adhesive for internal use can be found in the official FDA records.
Who is the listed applicant for Tissue adhesive for internal use?
The FDA 510(k) record lists Cohera Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tissue adhesive for internal use?
The FDA product code for Tissue adhesive for internal use is PJK.
相關臨床試驗
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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