ACE 电外科切除和气化电极系列
K号: K153055 · 2016-07-11
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器械摘要
常见问题
What is the ACE Electrosurgical Resection and Vaporization Electrodes Series?
ACE Electrosurgical Resection and Vaporization Electrodes Series is a medical device that received FDA 510(k) clearance on 2016-07-11. The listed applicant is Ace Medical Devices Pvt. , Ltd.. The 510(k) number is K153055.
When did ACE Electrosurgical Resection and Vaporization Electrodes Series receive FDA 510(k) clearance?
ACE Electrosurgical Resection and Vaporization Electrodes Series received FDA 510(k) clearance on 2016-07-11, under 510(k) number K153055.
Who is the listed applicant for ACE Electrosurgical Resection and Vaporization Electrodes Series?
The FDA 510(k) record lists Ace Medical Devices Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACE Electrosurgical Resection and Vaporization Electrodes Series?
The FDA product code for ACE Electrosurgical Resection and Vaporization Electrodes Series 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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