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FDA 510(k)

BiPad 手动激活,一次性双极电凝线

K号: K201833 · 2020-07-31

决定日期2020-07-31
产品代码GEI
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

BiPad Hand Activated, Disposable Bipolar Electrocautery Cords is the device name listed in this FDA 510(k) record. The listed applicant is Bipad Surgical, Inc.. It received FDA 510(k) clearance on 2020-07-31 under 510(k) number K201833. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BiPad Hand Activated, Disposable Bipolar Electrocautery Cords?

BiPad Hand Activated, Disposable Bipolar Electrocautery Cords is a medical device that received FDA 510(k) clearance on 2020-07-31. The listed applicant is Bipad Surgical, Inc.. The 510(k) number is K201833.

When did BiPad Hand Activated, Disposable Bipolar Electrocautery Cords receive FDA 510(k) clearance?

BiPad Hand Activated, Disposable Bipolar Electrocautery Cords received FDA 510(k) clearance on 2020-07-31, under 510(k) number K201833.

Who is the listed applicant for BiPad Hand Activated, Disposable Bipolar Electrocautery Cords?

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

What is the FDA product code for BiPad Hand Activated, Disposable Bipolar Electrocautery Cords?

The FDA product code for BiPad Hand Activated, Disposable Bipolar Electrocautery Cords is GEI.

相关临床试验

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。

相关器械(代码:GEI)

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。

官方来源

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