FDA 510(k)

Esophagus Bougie Set

K号: K161576 · 2016-10-02

决定日期2016-10-02

产品代码JAQ

咨询委员会RA

决定Substantially Equivalent

器械摘要

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.

常见问题

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.

列明Varian Medical Systems, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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