MEVION S250i 质子束放射治疗设备
K号: K172848 · 2017-12-27
广告
器械摘要
MEVION S250i Proton Beam Radiation Therapy Device is the device name listed in this FDA 510(k) record. The listed applicant is Mevion Medical Systems. It received FDA 510(k) clearance on 2017-12-27 under 510(k) number K172848. The device is classified under product code LHN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MEVION S250i Proton Beam Radiation Therapy Device?
MEVION S250i Proton Beam Radiation Therapy Device is a medical device that received FDA 510(k) clearance on 2017-12-27. The listed applicant is Mevion Medical Systems. The 510(k) number is K172848.
When did MEVION S250i Proton Beam Radiation Therapy Device receive FDA 510(k) clearance?
MEVION S250i Proton Beam Radiation Therapy Device received FDA 510(k) clearance on 2017-12-27, under 510(k) number K172848.
Who is the listed applicant for MEVION S250i Proton Beam Radiation Therapy Device?
The FDA 510(k) record lists Mevion Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEVION S250i Proton Beam Radiation Therapy Device?
The FDA product code for MEVION S250i Proton Beam Radiation Therapy Device is LHN.
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：LHN）
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。
K260597VIRTUE 质量认证ProNova SolutionsK260174PROBEAT-CRHitachi High-Tech Corp.K252815ProBeam 360 Proton Therapy System v3.0Varian Medical Systems, Inc.K253406S250-FIT 质子束放射治疗设备 (S250-FIT)Mevion Medical Systems, Inc.K250986S250-FIT 质子束放射治疗设备 (S250-FIT)Mevion Medical Systems, Inc.K243900eMotus 呼吸运动管理系统Empnia, Inc.
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