BiPad 手动激活,一次性双极电凝线
K号: K201833 · 2020-07-31
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器械摘要
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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