IBA质子治疗系统- Proteus 235（Proteus One，Proteus Plus，Proteus TK2，Proteus Class）
K号: K163500 · 2017-08-17
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器械摘要
常见问题
What is the IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class)?
IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class) is a medical device that received FDA 510(k) clearance on 2017-08-17. The listed applicant is Ion Beam Applications S.A.. The 510(k) number is K163500.
When did IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class) receive FDA 510(k) clearance?
IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class) received FDA 510(k) clearance on 2017-08-17, under 510(k) number K163500.
Who is the listed applicant for IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class)?
The FDA 510(k) record lists Ion Beam Applications S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class)?
The FDA product code for IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class) is LHN.
相关临床试验
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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。
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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