FDA 510(k)

Esophagus Bougie Set

K 號：K161576 · 2016-10-02

決定日期2016-10-02

產品代碼JAQ

諮詢委員會RA

決定Substantially Equivalent

器材摘要

Esophagus Bougie Set is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2016-10-02 under 510(k) number K161576. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Esophagus Bougie Set?

Esophagus Bougie Set is a medical device that received FDA 510(k) clearance on 2016-10-02. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K161576.

When did Esophagus Bougie Set receive FDA 510(k) clearance?

Esophagus Bougie Set received FDA 510(k) clearance on 2016-10-02, under 510(k) number K161576.

Who is the listed applicant for Esophagus Bougie Set?

The FDA 510(k) record lists Varian Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Esophagus Bougie Set?

The FDA product code for Esophagus Bougie Set is JAQ.

其他以 Varian Medical Systems, Inc. 為申請人之記錄

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相關器械（代碼：JAQ）

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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