gi2000 电外科发生器
K号: K250657 · 2025-06-03
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决定日期2025-06-03
产品代码GEI
咨询委员会SU
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器械摘要
gi2000 Electrosurgical Generator is the device name listed in this FDA 510(k) record. The listed applicant is Cintron Medical Corporation. It received FDA 510(k) clearance on 2025-06-03 under 510(k) number K250657. 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 gi2000 Electrosurgical Generator?
gi2000 Electrosurgical Generator is a medical device that received FDA 510(k) clearance on 2025-06-03. The listed applicant is Cintron Medical Corporation. The 510(k) number is K250657.
When did gi2000 Electrosurgical Generator receive FDA 510(k) clearance?
gi2000 Electrosurgical Generator received FDA 510(k) clearance on 2025-06-03, under 510(k) number K250657.
Who is the listed applicant for gi2000 Electrosurgical Generator?
The FDA 510(k) record lists Cintron Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for gi2000 Electrosurgical Generator?
The FDA product code for gi2000 Electrosurgical Generator 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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