組織切片針
K 號：K191472 · 2020-01-29
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器材摘要
Biopsy Needle is the device name listed in this FDA 510(k) record. The listed applicant is Ushare Medical, Inc.. It received FDA 510(k) clearance on 2020-01-29 under 510(k) number K191472. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Biopsy Needle?
Biopsy Needle is a medical device that received FDA 510(k) clearance on 2020-01-29. The listed applicant is Ushare Medical, Inc.. The 510(k) number is K191472.
When did Biopsy Needle receive FDA 510(k) clearance?
Biopsy Needle received FDA 510(k) clearance on 2020-01-29, under 510(k) number K191472.
Who is the listed applicant for Biopsy Needle?
The FDA 510(k) record lists Ushare Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Biopsy Needle?
The FDA product code for Biopsy Needle is FCG.
相關臨床試驗
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其他以 Ushare 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：FCG）
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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