Reedgyn一次性宮腔鏡（型號RH-2S-01及型號RH-2D-01）
K 號：K190797 · 2019-11-18
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器材摘要
常見問題
What is the Reedgyn disposable hysteroscope (Model RH-2S-01 and Model RH-2D-01)?
Reedgyn disposable hysteroscope (Model RH-2S-01 and Model RH-2D-01) is a medical device that received FDA 510(k) clearance on 2019-11-18. The listed applicant is Reed Medical (Zhejiang) Co., Ltd.. The 510(k) number is K190797.
When did Reedgyn disposable hysteroscope (Model RH-2S-01 and Model RH-2D-01) receive FDA 510(k) clearance?
Reedgyn disposable hysteroscope (Model RH-2S-01 and Model RH-2D-01) received FDA 510(k) clearance on 2019-11-18, under 510(k) number K190797.
Who is the listed applicant for Reedgyn disposable hysteroscope (Model RH-2S-01 and Model RH-2D-01)?
The FDA 510(k) record lists Reed Medical (Zhejiang) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reedgyn disposable hysteroscope (Model RH-2S-01 and Model RH-2D-01)?
The FDA product code for Reedgyn disposable hysteroscope (Model RH-2S-01 and Model RH-2D-01) is HIH.
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：HIH）
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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