电外科发生器ESG-150设备
K号: K182587 · 2018-11-29
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器械摘要
常见问题
What is the Device Electrosurgical Generator ESG-150?
Device Electrosurgical Generator ESG-150 is a medical device that received FDA 510(k) clearance on 2018-11-29. The listed applicant is Olympus Winter & Ibe GmbH. The 510(k) number is K182587.
When did Device Electrosurgical Generator ESG-150 receive FDA 510(k) clearance?
Device Electrosurgical Generator ESG-150 received FDA 510(k) clearance on 2018-11-29, under 510(k) number K182587.
Who is the listed applicant for Device Electrosurgical Generator ESG-150?
The FDA 510(k) record lists Olympus Winter & Ibe GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Device Electrosurgical Generator ESG-150?
The FDA product code for Device Electrosurgical Generator ESG-150 is GEI.
相关临床试验
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列明Olympus Winter & Ibe GmbH为申报人的其他记录
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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