DOOPANG
K 號：K232749 · 2024-06-11
廣告
器材摘要
DOOPANG is the device name listed in this FDA 510(k) record. The listed applicant is Ybrain, Inc.. It received FDA 510(k) clearance on 2024-06-11 under 510(k) number K232749. The device is classified under product code PCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the DOOPANG?
DOOPANG is a medical device that received FDA 510(k) clearance on 2024-06-11. The listed applicant is Ybrain, Inc.. The 510(k) number is K232749.
When did DOOPANG receive FDA 510(k) clearance?
DOOPANG received FDA 510(k) clearance on 2024-06-11, under 510(k) number K232749.
Who is the listed applicant for DOOPANG?
The FDA 510(k) record lists Ybrain, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOOPANG?
The FDA product code for DOOPANG is PCC.
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。
相關器械（代碼：PCC）
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。
K254216Enso 頭痛用藥品Hinge Health, Inc.K242719ELEXIR 2.0 (ALLIVE3)Nu Eyne Co., Ltd.K234029CEFALY 連接 - 非處方藥，CEFALY 連接 - 藥局處方Cefaly TechnologyK233751米維爾（YPS-301BD）Soterix Medical, Inc.K230782TENS設備-HeadaTerm 2（型號：YF-HT2）Wat Medical Technology, Inc.K212071Cefaly雙效強化版配RFID - 非處方藥，Cefaly雙效強化版配RFID - 藥局處方，Cefaly雙連接版 - 非處方藥，Cefaly雙連接版 - 藥局處方Cefaly Technology
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。
廣告