ASEPT 腹膜引流系統
K 號：K221779 · 2023-05-02
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器材摘要
ASEPT Peritoneal Drainage System is the device name listed in this FDA 510(k) record. The listed applicant is Pfm Medical, Inc.. It received FDA 510(k) clearance on 2023-05-02 under 510(k) number K221779. The device is classified under product code PNG. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
常見問題
What is the ASEPT Peritoneal Drainage System?
ASEPT Peritoneal Drainage System is a medical device that received FDA 510(k) clearance on 2023-05-02. The listed applicant is Pfm Medical, Inc.. The 510(k) number is K221779.
When did ASEPT Peritoneal Drainage System receive FDA 510(k) clearance?
ASEPT Peritoneal Drainage System received FDA 510(k) clearance on 2023-05-02, under 510(k) number K221779.
Who is the listed applicant for ASEPT Peritoneal Drainage System?
The FDA 510(k) record lists Pfm Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASEPT Peritoneal Drainage System?
The FDA product code for ASEPT Peritoneal Drainage System is PNG.
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。
其他以 Pfm Medical, Inc. 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：PNG）
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
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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