Monteris Medical NeuroBlate 系统
K号: K240877 · 2024-06-04
广告
器械摘要
Monteris Medical NeuroBlate System is the device name listed in this FDA 510(k) record. The listed applicant is Monteris Medical,. It received FDA 510(k) clearance on 2024-06-04 under 510(k) number K240877. The device is classified under product code ONO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Monteris Medical NeuroBlate System?
Monteris Medical NeuroBlate System is a medical device that received FDA 510(k) clearance on 2024-06-04. The listed applicant is Monteris Medical,. The 510(k) number is K240877.
When did Monteris Medical NeuroBlate System receive FDA 510(k) clearance?
Monteris Medical NeuroBlate System received FDA 510(k) clearance on 2024-06-04, under 510(k) number K240877.
Who is the listed applicant for Monteris Medical NeuroBlate System?
The FDA 510(k) record lists Monteris Medical, as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Monteris Medical NeuroBlate System?
The FDA product code for Monteris Medical NeuroBlate System is ONO.
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。
列明Monteris Medical,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：ONO）
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。
K262315NeuroBlate 系统Monteris MedicalK260976NeuroBlate 系统Monteris MedicalK253391Visualase 冷却激光治疗仪系统（9735559）；Visualase 冷却激光治疗仪系统（9735560）；Visualase 冷却激光治疗仪系统（9735561）Medtronic Navigation, Inc.K251298移动激光单元（1001-N2）；Thermoguide 工作站（1100-N1）；激光应用器（4012-N5，4017-N2，4017-N4）；MR 引导器（4013-N6）Clinical Laserthermia Systems, ABK250307Visualase V2 MRI引导激光消融系统（9736422）Medtronic NavigationK214125TRANBERG 热导治疗系统Clinical Laserthermia Systems, AB
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。
广告