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FDA 510(k)

U 達爾維爾 Bolink ENFit 結合輸食組

K 號:K170555 · 2017-08-17

決定日期2017-08-17
產品代碼PIF
諮詢委員會GU
決定相當於

器材摘要

U Deliver Bolink ENFit Enteral Feeding Sets is the device name listed in this FDA 510(k) record. The listed applicant is U Deliver Medical, LLC. It received FDA 510(k) clearance on 2017-08-17 under 510(k) number K170555. The device is classified under product code PIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the U Deliver Bolink ENFit Enteral Feeding Sets?

U Deliver Bolink ENFit Enteral Feeding Sets is a medical device that received FDA 510(k) clearance on 2017-08-17. The listed applicant is U Deliver Medical, LLC. The 510(k) number is K170555.

When did U Deliver Bolink ENFit Enteral Feeding Sets receive FDA 510(k) clearance?

U Deliver Bolink ENFit Enteral Feeding Sets received FDA 510(k) clearance on 2017-08-17, under 510(k) number K170555.

Who is the listed applicant for U Deliver Bolink ENFit Enteral Feeding Sets?

The FDA 510(k) record lists U Deliver Medical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for U Deliver Bolink ENFit Enteral Feeding Sets?

The FDA product code for U Deliver Bolink ENFit Enteral Feeding Sets is PIF.

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。

其他以 U Deliver Medical, LLC 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:PIF)

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

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