← Product Code [LLZ](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ) · K092741 # COLOR LCD MONITOR, MODEL RADIFORCE MX241W (K092741) _Eizo Nanao Corporation · LLZ · Nov 10, 2009 · Radiology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ/K092741 ## Device Facts - **Applicant:** Eizo Nanao Corporation - **Product Code:** [LLZ](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ.md) - **Decision Date:** Nov 10, 2009 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 892.2050 - **Device Class:** Class 2 - **Review Panel:** Radiology ## Intended Use RadiForce MX241W is intended to be used in displaying and viewing digital images for diagnosis of X-ray or MRI, etc. by trained medical practitioners. The device is not specified for digital mammography system. ## Device Story RadiForce MX241W is a 61cm (24.1") color LCD monitor for medical image viewing. Used by trained medical practitioners in clinical settings to display digital images (X-ray, MRI). Device receives digital image data from medical imaging workstations; displays images for diagnostic review. Features improved brightness (320 cd/m2) and DisplayPort input compared to predicate. Does not support mammography. Provides high-resolution visualization to assist clinicians in diagnostic decision-making. ## Clinical Evidence No clinical data. Bench testing only. ## Technological Characteristics Color LCD monitor; 61cm (24.1") display panel; 320 cd/m2 brightness; DisplayPort input terminal. Standalone medical display device. ## Regulatory Identification A medical image management and processing system is a device that provides one or more capabilities relating to the review and digital processing of medical images for the purposes of interpretation by a trained practitioner of disease detection, diagnosis, or patient management. The software components may provide advanced or complex image processing functions for image manipulation, enhancement, or quantification that are intended for use in the interpretation and analysis of medical images. Advanced image manipulation functions may include image segmentation, multimodality image registration, or 3D visualization. Complex quantitative functions may include semi-automated measurements or time-series measurements. ## Special Controls *Classification.* Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern). ## Predicate Devices - FlexScan MX300W ([K073340](/device/K073340.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ K092 741 ### 510(k) Summary as required by 807.92 - 1. Company Identification NOV 1 0 2009 EIZO NANAO CORPORATION 153 Shimokashiwano-cho, Hakusan, Ishikawa-ken, 924-8566, Japan Tel: +81-76-274-2468 Fax: +81-76-274-2484 - 2. Official Correspondent Hiroaki Hashimoto (Mr.) Manager of Engineering Management Section 3. Date of Submission September 4, 2009 - 4. Device Trade name Color LCD Monitor, RadiForce MX241W - 5. Common/Usual Name: Image display system, medical image workstation, image monitor/display, and others - 6. Classification Number: Medical displays classified in Class II per 21 CFR 892.2050. #### 7. Predicate Device | | Manufacturer | : EIZO NANAO CORPORATION | |-------------|--------------|--------------------------| | Device Name | | : Color LCD Monitor | | Model Name | | : FlexScan MX300W | | 510(k) No. | | : K073340 | - 8. Description of Device RadiForce MX241W is 61cm Color LCD display for medical image viewing digital images viewing. - 9. Intended Use RadiForce MX241W is intended to be used in displaying and viewing digital images for diagnosis of X-ray or MRI, etc. by trained medical practitioners. The device is not specified for digital mammography system. - 10. Substantial Equivalence to Predicate Device RadiForce MX241W is substantially equivalent to FlexScan MX300W (K073340). The panel size is changed to 61 cm (24.1") from 76cm (29.8"). MX241W improved the brightness. The brightness improved to 320 cd/m2 from 300 cd/m2. DisplayPort is added as new input terminal. Comparison table of the principal characteristics of 2 devices is shown in the Attachment 1. Appendix 1: Comparison Table with Predicate Device {1}------------------------------------------------ Image /page/1/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of the department's name arranged in a circular fashion around a stylized eagle. The eagle is depicted with its wings spread, and its head turned to the left. The text reads "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA". ### DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Room - WO66-G609 Silver Spring, MD 20993-0002 ## NOV 1 0 2009 Mr. Hiroaki Hashimoto Manager EIZO NANAO Corporation, Engineering Management Section 153 Shimokashiwano-cho, Hakusan, Ishikawa-ken 924-8566 JAPAN Re: K092741 Trade/Device Name: Color LCD Monitor, RadiForce MX241W Regulation Number: 21 CFR 892.2050 Regulation Name: Picture archiving and communications system Regulatory Class: II Product Code: LLZ Dated: October 21, 2009 Received: October 22, 2009 Dear Mr. Hashimoto: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices. good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical {2}------------------------------------------------ Page 2 - Enclosure device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.html Sincerely yours, Janine M. Morris Acting Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health {3}------------------------------------------------ # Indications for Use K092741 (k) Number: K092741 ëvice Name . . Color LCD Monitor, RadiForce MX241W dications for Use: RadiForce MX241W is intended to be used in displaying and viewing digital images for Radil ore MX24117 - Is there and medical practitioners. RadiForce MX241W does not support the display of mammography images for diagnosis. escription Use art 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) EASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Aorri m. Wh Division of Reproductive, Abdominal and Radiological Dev 510(k) Number --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ/K092741](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ/K092741) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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