MicroFrance Monopolar and Bipolar Electrosurgical Instruments
K号: K210942 · 2021-05-14
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器械摘要
常见问题
What is the MicroFrance Monopolar and Bipolar Electrosurgical Instruments?
MicroFrance Monopolar and Bipolar Electrosurgical Instruments is a medical device that received FDA 510(k) clearance on 2021-05-14. The listed applicant is Integra Microfrance. The 510(k) number is K210942.
When did MicroFrance Monopolar and Bipolar Electrosurgical Instruments receive FDA 510(k) clearance?
MicroFrance Monopolar and Bipolar Electrosurgical Instruments received FDA 510(k) clearance on 2021-05-14, under 510(k) number K210942.
Who is the listed applicant for MicroFrance Monopolar and Bipolar Electrosurgical Instruments?
The FDA 510(k) record lists Integra Microfrance as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MicroFrance Monopolar and Bipolar Electrosurgical Instruments?
The FDA product code for MicroFrance Monopolar and Bipolar Electrosurgical Instruments is GEI.
相关临床试验
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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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