电外科手术发生器及附件
K号: K201224 · 2020-09-18
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器械摘要
Electrosurgical Generator and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Medrange. It received FDA 510(k) clearance on 2020-09-18 under 510(k) number K201224. 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 Electrosurgical Generator and Accessories?
Electrosurgical Generator and Accessories is a medical device that received FDA 510(k) clearance on 2020-09-18. The listed applicant is Medrange. The 510(k) number is K201224.
When did Electrosurgical Generator and Accessories receive FDA 510(k) clearance?
Electrosurgical Generator and Accessories received FDA 510(k) clearance on 2020-09-18, under 510(k) number K201224.
Who is the listed applicant for Electrosurgical Generator and Accessories?
The FDA 510(k) record lists Medrange as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electrosurgical Generator and Accessories?
The FDA product code for Electrosurgical Generator and Accessories 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。
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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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