FDA 510(k)

腸內輸液泵針筒

K 號：K211593 · 2021-09-30

決定日期2021-09-30

產品代碼PNR

諮詢委員會GU

決定相當於

器材摘要

Enteral Pump Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Caina Medical Co.,Ltd. It received FDA 510(k) clearance on 2021-09-30 under 510(k) number K211593. The device is classified under product code PNR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Enteral Pump Syringe?

Enteral Pump Syringe is a medical device that received FDA 510(k) clearance on 2021-09-30. The listed applicant is Jiangsu Caina Medical Co.,Ltd. The 510(k) number is K211593.

When did Enteral Pump Syringe receive FDA 510(k) clearance?

Enteral Pump Syringe received FDA 510(k) clearance on 2021-09-30, under 510(k) number K211593.

Who is the listed applicant for Enteral Pump Syringe?

The FDA 510(k) record lists Jiangsu Caina Medical Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Enteral Pump Syringe?

The FDA product code for Enteral Pump Syringe is PNR.

其他以 Jiangsu Caina Medical Co.,Ltd 為申請人之記錄

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相關器械（代碼：PNR）

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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