510(k) K241441

Device
RadiForce RX670; RadiForce RX670-AR
Applicant
Eizo Corporation
510(k) number
K241441
Product code
PGY
Decision
Substantially Equivalent (SESE)
Decision date
2024-07-16
Date received
2024-05-22
Regulation
892.2050
Classification name
Display, Diagnostic Radiology
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Hiroaki Hashimoto
Address
153 Shimokashiwano Hakusan, Ishikawa JP 924-8566 924-8566

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
04995047067269RadiForce®EIZO CORPORATION2024-08-01
04995047067184RadiForce®EIZO CORPORATION2024-08-01

Other 510(k) Records For Product Code PGY

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K240310LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.2024-03-29
K240130Medical Monitor (21HQ613D)Lg Electronics.Inc2024-02-15
K2338975MP Color LCD Monitors/ 5MP Monochrome LCD Monitors (C510S, G510S, CB5MP, MB5MP, C516S, G516S)Shenzhen Beacon Display Technology Co., Ltd.2024-02-06
K233465RadiForce MX317WEizo Corporation2023-12-21
K23298524HR513CLg Electronics.Inc2023-12-11
K233693Nio Color 8MP (MDNC-8132)Barco N.V.2023-12-11