PowerGlide Pro Midline Catheter
K 號：K162377 · 2016-09-22
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器材摘要
PowerGlide Pro Midline Catheter 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 2016-09-22 under 510(k) number K162377. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the PowerGlide Pro Midline Catheter?
PowerGlide Pro Midline Catheter is a medical device that received FDA 510(k) clearance on 2016-09-22. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162377.
When did PowerGlide Pro Midline Catheter receive FDA 510(k) clearance?
PowerGlide Pro Midline Catheter received FDA 510(k) clearance on 2016-09-22, under 510(k) number K162377.
Who is the listed applicant for PowerGlide Pro Midline Catheter?
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 PowerGlide Pro Midline Catheter?
The FDA product code for PowerGlide Pro Midline Catheter is FOZ.
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其他以 C.R. Bard, Inc. 為申請人之記錄
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相關器械（代碼：FOZ）
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
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