Pinpoint GT Introducer Needle
K 號：K162769 · 2016-11-04
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器材摘要
Pinpoint GT Introducer Needle is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2016-11-04 under 510(k) number K162769. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Pinpoint GT Introducer Needle?
Pinpoint GT Introducer Needle is a medical device that received FDA 510(k) clearance on 2016-11-04. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162769.
When did Pinpoint GT Introducer Needle receive FDA 510(k) clearance?
Pinpoint GT Introducer Needle received FDA 510(k) clearance on 2016-11-04, under 510(k) number K162769.
Who is the listed applicant for Pinpoint GT Introducer Needle?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pinpoint GT Introducer Needle?
The FDA product code for Pinpoint GT Introducer Needle is DYB.
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其他以 C.R. Bard, 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。
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相關器械（代碼：DYB）
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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