Bovie一次性双极消融器
K号: K152777 · 2016-01-15
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器械摘要
常见问题
What is the Bovie Disposable Bipolar Ablator?
Bovie Disposable Bipolar Ablator is a medical device that received FDA 510(k) clearance on 2016-01-15. The listed applicant is Bovie Medical Corporation. The 510(k) number is K152777.
When did Bovie Disposable Bipolar Ablator receive FDA 510(k) clearance?
Bovie Disposable Bipolar Ablator received FDA 510(k) clearance on 2016-01-15, under 510(k) number K152777.
Who is the listed applicant for Bovie Disposable Bipolar Ablator?
The FDA 510(k) record lists Bovie Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bovie Disposable Bipolar Ablator?
The FDA product code for Bovie Disposable Bipolar Ablator is GEI.
相关临床试验
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列明Bovie Medical Corporation为申报人的其他记录
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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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