CW60N
K号: K222722 · 2022-10-31
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器械摘要
CW60N is the device name listed in this FDA 510(k) record. The listed applicant is Wide Corporation. It received FDA 510(k) clearance on 2022-10-31 under 510(k) number K222722. 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 CW60N?
CW60N is a medical device that received FDA 510(k) clearance on 2022-10-31. The listed applicant is Wide Corporation. The 510(k) number is K222722.
When did CW60N receive FDA 510(k) clearance?
CW60N received FDA 510(k) clearance on 2022-10-31, under 510(k) number K222722.
Who is the listed applicant for CW60N?
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 CW60N?
The FDA product code for CW60N 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。
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