RadiForce RX570; RadiForce RX570-AR
K号: K243221 · 2024-11-27
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器械摘要
RadiForce RX570; RadiForce RX570-AR is the device name listed in this FDA 510(k) record. The listed applicant is Eizo Corporation. It received FDA 510(k) clearance on 2024-11-27 under 510(k) number K243221. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the RadiForce RX570; RadiForce RX570-AR?
RadiForce RX570; RadiForce RX570-AR is a medical device that received FDA 510(k) clearance on 2024-11-27. The listed applicant is Eizo Corporation. The 510(k) number is K243221.
When did RadiForce RX570; RadiForce RX570-AR receive FDA 510(k) clearance?
RadiForce RX570; RadiForce RX570-AR received FDA 510(k) clearance on 2024-11-27, under 510(k) number K243221.
Who is the listed applicant for RadiForce RX570; RadiForce RX570-AR?
FDA 510(k)记录中列出Eizo Corporation为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for RadiForce RX570; RadiForce RX570-AR?
The FDA product code for RadiForce RX570; RadiForce RX570-AR is PGY.
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Eizo Corporation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：PGY）
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。
K262783RadiForce MX247WEizo CorporationK261213医用监护仪（40HT513D）Lg Electronics.IncK252780LCD 显示器 (CL1902A, CL2103F)Shenzhen Beacon Display Technology Co., Ltd.K253242LCD 显示器 (C1216W, C822W, C821W)Shenzhen Beacon Display Technology Co., Ltd.K252030RadiForce GX570; RadiForce GX570-AREizo CorporationK243031LCD 显示器 C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., 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。
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