CX50N(CX50YQS)
K号: K170783 · 2017-03-31
广告
器械摘要
CX50N(CX50YQS) is the device name listed in this FDA 510(k) record. The listed applicant is Wide Corporation. It received FDA 510(k) clearance on 2017-03-31 under 510(k) number K170783. 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 CX50N(CX50YQS)?
CX50N(CX50YQS) is a medical device that received FDA 510(k) clearance on 2017-03-31. The listed applicant is Wide Corporation. The 510(k) number is K170783.
When did CX50N(CX50YQS) receive FDA 510(k) clearance?
CX50N(CX50YQS) received FDA 510(k) clearance on 2017-03-31, under 510(k) number K170783.
Who is the listed applicant for CX50N(CX50YQS)?
The FDA 510(k) record lists Wide Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CX50N(CX50YQS)?
The FDA product code for CX50N(CX50YQS) is PGY.
列明Wide 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 CorporationK243221RadiForce RX570; RadiForce RX570-AREizo Corporation
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