FDA 510(k)

Sunmed 控制針筒

K 號：K160190 · 2016-11-10

申請人Sunny Medical Device (Shenzhen) Co., Ltd.

決定日期2016-11-10

產品代碼DXT

諮詢委員會履歷

決定相當於

器材摘要

Sunmed Control Syringes is the device name listed in this FDA 510(k) record. The listed applicant is Sunny Medical Device (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2016-11-10 under 510(k) number K160190. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Sunmed Control Syringes?

Sunmed Control Syringes is a medical device that received FDA 510(k) clearance on 2016-11-10. The listed applicant is Sunny Medical Device (Shenzhen) Co., Ltd.. The 510(k) number is K160190.

When did Sunmed Control Syringes receive FDA 510(k) clearance?

Sunmed Control Syringes received FDA 510(k) clearance on 2016-11-10, under 510(k) number K160190.

Who is the listed applicant for Sunmed Control Syringes?

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

What is the FDA product code for Sunmed Control Syringes?

The FDA product code for Sunmed Control Syringes is DXT.

其他以 Sunny Medical Device (Shenzhen) Co., Ltd. 為申請人之記錄

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K191827Sunmed 一次性動脈閉合墊 K153685Sunmed 止血閥

相關器械（代碼：DXT）

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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