iMac 27 & PL 4.0
K号: K200889 · 2020-06-02
广告
器械摘要
iMac 27 & PL 4.0 is the device name listed in this FDA 510(k) record. The listed applicant is Quantum-Spectra, LLC. It received FDA 510(k) clearance on 2020-06-02 under 510(k) number K200889. 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 iMac 27 & PL 4.0?
iMac 27 & PL 4.0 is a medical device that received FDA 510(k) clearance on 2020-06-02. The listed applicant is Quantum-Spectra, LLC. The 510(k) number is K200889.
When did iMac 27 & PL 4.0 receive FDA 510(k) clearance?
iMac 27 & PL 4.0 received FDA 510(k) clearance on 2020-06-02, under 510(k) number K200889.
Who is the listed applicant for iMac 27 & PL 4.0?
The FDA 510(k) record lists Quantum-Spectra, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iMac 27 & PL 4.0?
The FDA product code for iMac 27 & PL 4.0 is PGY.
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