PROBEAT-CR
K号: K260174 · 2026-06-11
广告
器械摘要
PROBEAT-CR is the device name listed in this FDA 510(k) record. The listed applicant is Hitachi High-Tech Corp.. It received FDA 510(k) clearance on 2026-06-11 under 510(k) number K260174. 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 PROBEAT-CR?
PROBEAT-CR is a medical device that received FDA 510(k) clearance on 2026-06-11. The listed applicant is Hitachi High-Tech Corp.. The 510(k) number is K260174.
When did PROBEAT-CR receive FDA 510(k) clearance?
PROBEAT-CR received FDA 510(k) clearance on 2026-06-11, under 510(k) number K260174.
Who is the listed applicant for PROBEAT-CR?
The FDA 510(k) record lists Hitachi High-Tech Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROBEAT-CR?
The FDA product code for PROBEAT-CR 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 SolutionsK252815ProBeam 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.K242418P-Cure质子治疗系统（PPTS）P-Cure, Ltd.
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