FDA 510(k)

威戈-不锈钢

K号: K193209 · 2020-02-19

决定日期2020-02-19

产品代码GAQ

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决定实质等同

器械摘要

Wego-Stainless Steel is the device name listed in this FDA 510(k) record. The listed applicant is Foosin Medical Supplies Inc., Ltd.. It received FDA 510(k) clearance on 2020-02-19 under 510(k) number K193209. The device is classified under product code GAQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Wego-Stainless Steel?

Wego-Stainless Steel is a medical device that received FDA 510(k) clearance on 2020-02-19. The listed applicant is Foosin Medical Supplies Inc., Ltd.. The 510(k) number is K193209.

When did Wego-Stainless Steel receive FDA 510(k) clearance?

Wego-Stainless Steel received FDA 510(k) clearance on 2020-02-19, under 510(k) number K193209.

Who is the listed applicant for Wego-Stainless Steel?

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

What is the FDA product code for Wego-Stainless Steel?

The FDA product code for Wego-Stainless Steel is GAQ.

列明Foosin Medical Supplies Inc., Ltd.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。

K201139WEGO-PDO 刺激缝合线 K183004WEGO-PGA 快速 K183001WEGO-PGLA 快速 K170842WEGO-PTFE

官方来源

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