6MP Color LCD Monitor, RadiForce RX660, RX660-AR

K163335 · Eizo Corporation · PGY · Dec 15, 2016 · Radiology

Device Facts

• Record ID: K163335
• Device Name: 6MP Color LCD Monitor, RadiForce RX660, RX660-AR
• Applicant: Eizo Corporation
• Product Code: PGY · Radiology
• Decision Date: Dec 15, 2016
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.2050
• Device Class: Class 2

Indications for Use

This product is intended to be used in displaying digital images for review, analysis and diagnosis by trained medical practitioners. It does not support the display of mammography images for diagnosis.

Device Story

The RadiForce RX660/RX660-AR is a 6MP color LCD monitor designed for clinical review, analysis, and diagnosis of medical images (excluding mammography). It utilizes an IPS panel with 3,280 x 2,048 resolution. The device receives digital video signals via DVI-D or DisplayPort from a workstation. Internal lookup tables store factory-calibrated display modes, including DICOM GSDF compliance, ensuring consistent tone curves regardless of the display controller. The RX660 features an anti-glare surface, while the RX660-AR features an anti-reflection coating. The monitor includes integrated sensors (backlight, front, presence, and ambient light) for automated quality control. RadiCS software, installed on the host workstation, manages quality control, performing quantitative and visual tests. Healthcare providers use the monitor to view high-resolution medical imagery; the device's calibrated luminance and uniformity support accurate diagnostic interpretation. The system is intended for use in clinical environments by trained medical professionals.

Clinical Evidence

No clinical or animal testing was performed. Substantial equivalence is supported by bench testing, including verification of DICOM GSDF conformance, luminance and chromaticity non-uniformity measurements, MTF spatial resolution assessment, and visual artifact checks per AAPM TG18 guidelines.

Technological Characteristics

TFT Color LCD Panel (IPS); 6MP (3,280 x 2,048) resolution; LED backlighting; 1,000 cd/m² max luminance; 1500:1 contrast ratio; 25ms response time. Connectivity: DVI-D (dual link) and DisplayPort. Integrated sensors: backlight, front, presence, and ambient light. Digital Uniformity Equalizer for luminance compensation. Software: RadiCS for quality control. Power: 100-240V AC.

Indications for Use

Indicated for trained medical practitioners to display and view digital images for review, analysis, and diagnosis. Not indicated for the display of mammography images.

Regulatory Classification

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

• RadiForce RX650 (K134002)

Submission Summary (Full Text)

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Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

December 15, 2016

EIZO Corporation % Mr. Hiroaki Hashimoto Manager, Medical System Standards 153 Shimokashiwano Hakusan, Ishikawa 924-8566 JAPAN

Re: K163335

Trade/Device Name: 6MP Color LCD Monitor, RadiForce RX660, RX660-AR Regulation Number: 21 CFR 892.2050 Regulation Name: Picture archiving and communications system Regulatory Class: II Product Code: PGY Dated: November 24, 2016 Received: November 28, 2016

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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

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 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.

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If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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 Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely yours.

Michael D'Hara

For

Robert Ochs, Ph.D. Director Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health

Enclosure

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# Indications for Use

510(k) Number (if known) K163335

Device Name

6MP Color LCD Monitor, RadiForce RX660, RX660-AR

Indications for Use (Describe)

This product is intended to be used in displaying digital images for review, analysis and diagnosis by trained medical practitioners. It does not support the display of mammography images for diagnosis.

Type of Use (Select one or both, as applicable)

X Prescription Use (Part 21 CFR 801 Subpart D)

| Over-The-Counter Use (21 CFR 801 Subpart C)

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Image /page/3/Picture/0 description: The image shows the logo for EIZO. The logo consists of a stylized square shape on the left and the word "EIZO" in bold, sans-serif font on the right. The square shape is divided into smaller squares, some of which are filled in with a darker color, creating a checkered pattern. A small registered trademark symbol is located to the upper right of the letter "O".

EIZO Corporation, 153 Shimokashiwano, Hakusan, Ishikawa 924-8566 Japan

U.S. Food and Drug Administration Center for Devices and Radiological Health Document Mail Center - WO66-G609 10903 New Hampshire Avenue Silver Spring, MD 20993-0002

Hiroaki Hashimoto Name Department Medical System Standards

Telephone [phone] Fax E-Mail

# [phone] [e-mail]

# 510(k) Summary (in accordance with 21 CFR 807.92)

#### 1. Company

EIZO Corporation 153 Shimokashiwano, Hakusan Ishikawa 924-8566 Japan Tel: [phone] Fax: [phone]

# 2. Contact Person

Hiroaki Hashimoto

#### 3. Date of Summary November 24th, 2016

#### 4. Device Information

- Device Name: 6MP Color LCD Monitor, RadiForce RX660, RX660-AR
- Trade Name/Model: RadiForce RX660, RX660-AR ●
- Common Name: 6MP Color LCD Monitor ●
- Classification Name: ● Display, Diagnostic Radiology
- Regulation Number: 21 CFR 892.2050, Product Code PGY ●

#### 5. Predicate Device

6MP Color LCD Monitor, RadiForce RX650 (K134002)

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# 6. Device Description

RadiForce RX660 is a color LCD monitor for viewing medical images other than those of mammography. The color panel employs in-plane switching (IPS) technology allowing wide viewing angles and the matrix size (or resolution) is 3,280 x 2,048 pixels (6MP) with a pixel pitch of 0.1968 mm.

Since factory calibrated display modes, each of which is characterized by a specific tone curve (including DICOM GSDF), a specific luminance range and a specific color temperature, are stored in lookup tables within the monitor, the tone curve is e.g. DICOM compliant regardless of the display controller used.

There are two model variations, RX660 and RX660-AR. The difference of the two variations is the surface treatment of the display screens; the surface treatment of the RX660 is Anti-Glare (AG) treatment and that of the RX660-AR is Anti-Reflection (AR) coating.

RadiCS is application software to be installed in each workstation offering worry-free quality control of the diagnostic monitors including the RadiForce RX660 based on the QC standards and guidelines and is capable of quantitative tests and visual tests defined by them. The RadiCS and its subset, RadiCS LE, are included in this 510(k) submission as an accessory to the RadiForce RX660.

#### 7. Indications for use

This product is intended to be used in displaying and viewing digital images for review, analysis and diagnosis by trained medical practitioners. It does not support the display of mammography images for diagnosis.

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# 8. Comparison of Technological Characteristics

The comparison table below enumerates information derived from the product brochure of the each device and different technological characteristics are discussed in it:

| Attributes | RadiForce RX660 | RadiForce RX650 | Explanation of<br>Differences | | | | | | | | |
|-------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------|------------------------|-------------------------------------------|------------------------------------------------------------------------|---|-------------------------|----------------------------------|--|---|
| Display Performance/Specifications | | | | | | | | | | | |
| Screen<br>technology | TFT Color<br>LCD Panel (IPS) | TFT Color<br>LCD Panel (IPS) | - | | | | | | | | |
| Viewing angle<br>(H, V) | H: 176°, V: 176° | H: 176°, V: 176° | - | | | | | | | | |
| Resolution | 6MP (3,280 x 2,048) | 6MP (3,280 x 2,048) | - | | | | | | | | |
| Aspect ratio | 16:10 | 16:10 | - | | | | | | | | |
| Active screen<br>size | 645.5 mm x 403.0 mm | 645.5 mm x 403.0 mm | - | | | | | | | | |
| Pixel pitch | 0.1968 mm x 0.1968 mm | 0.197 mm x 0.197 mm | - | | | | | | | | |
| Maximum<br>luminance | 1,000 cd/m² | 800 cd/m² | - | | | | | | | | |
| DICOM<br>calibrated<br>luminance | 500 cd/m² | 400 cd/m² | - | | | | | | | | |
| Contrast ratio | 1500 : 1 | 1000:1 | - | | | | | | | | |
| Response<br>Time (typical) | 25 ms (On/Off) | 30 ms (On/Off) | - | | | | | | | | |
| Backlighting | LED | LED | - | | | | | | | | |
| Display Colors | From a palette of 68<br>billion colors:<br>- 10-bit (DisplayPort):<br>1.07 billion colors<br>(maximum)<br>- 8-bit colors: 16.77<br>million colors | From a palette of 68 billion<br>colors:<br>- 10-bit (DisplayPort): 1.07<br>billion colors (maximum)<br>- 8-bit colors: 16.77 million<br>colors | - | | | | | | | | |
| Luminance<br>non-<br>uniformity<br>compensation | Digital Uniformity<br>Equalizer | Digital Uniformity<br>Equalizer | - | | | | | | | | |
| Video Signals | | | | Input video<br>signals | DVI-D (dual link) x 1,<br>DisplayPort x 2 | DVI-D (dual link) x 2,<br>DisplayPort x 2<br>(two inputs are required) | - | Output video<br>signals | DisplayPort x 1 (daisy<br>chain) | | - |
| Video Signals | | | | | | | | | | | |
| Input video<br>signals | DVI-D (dual link) x 1,<br>DisplayPort x 2 | DVI-D (dual link) x 2,<br>DisplayPort x 2<br>(two inputs are required) | - | | | | | | | | |
| Output video<br>signals | DisplayPort x 1 (daisy<br>chain) | | - | | | | | | | | |

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| Scanning<br>Frequency (H,<br>V) | 31 - 127 kHz / 22 - 61 Hz<br>(VGA Text: 69 - 71 Hz)<br>Frame synchronous mode:<br>29.5 - 30.5 Hz, 59 - 61<br>Hz | 31 - 129 kHz / 29 - 61 Hz<br>(VGA Text: 69 - 71 Hz)<br>Frame synchronous mode:<br>29.5 - 30.5 Hz, 59 - 61 Hz | |
|----------------------------------------|-----------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------|------------------------------|
| Power Related Specifications | | | |
| Power<br>Requirements | AC 100 - 240 V:<br>50 / 60 Hz | AC 100 - 120 V,<br>200 - 240 V: 50 / 60 Hz | |
| Power<br>Consumption /<br>Save Mode | 190 W / Less than 1.6 W | 225 W / Less than 6 W | |
| Power<br>Management | DVI DMPM,<br>DisplayPort 1.2a | DVI DMPM,<br>DisplayPort 1.1a | |
| Miscellaneous Features/Specifications | | | |
| QC software | RadiCS | RadiCS | |
| Sensors | Backlight Sensor,<br>Integrated Front Sensor,<br>Presence Sensor,<br>Ambient Light Sensor | Backlight Sensor,<br>Integrated Front Sensor,<br>Presence Sensor,<br>Ambient Light Sensor | |
| USB Ports /<br>Standard | 2 upstream,<br>3 downstream / Rev. 2.0 | 1 upstream,<br>2 downstream / Rev. 2.0 | |
| Dimensions<br>w/o stand<br>(W x H x D) | 682.5 x 441 x 88 mm | 692 x 466 x 109 mm | Different housing<br>design. |

It is clear that the technological characteristics differences discussed above do not affect the safety and the effectiveness of the RX660.

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## 9. Performance Testing

The following bench tests were performed on the RadiForce RX660.

- . Verification of the conformance to DICOM GSDF as specified in Assessment of Display Performance for Medical Imaging Systems by AAPM Task Group 18 (TG18 guideline)
- . Measurement of the luminance non-uniformity characteristics of the display screen as specified in TG18 guideline
- . Measurement of the chromaticity non-uniformity characteristics of the display screen as specified in TG18 guideline
- . Measurement of the chromaticity at the center of the display screen at 5%, 50% and 95% of the maximum luminance
- . Visual check of presence or absence of miscellaneous artifacts on the display screen as specified in TG18 guideline
- . Measurement of spatial resolution expressed as modulation transfer function (MTF)
- The maximum number allowed for each type of pixel defects/faults

The test results showed that the RadiForce RX660 has display characteristics equivalent to those of the predicate device. RadiForce RX650.

Besides, the display characteristics of the RadiForce RX660 meet the pre-defined criteria when criteria are set.

No animal or clinical testing was performed on the RadiForce RX660.

#### 10. Conclusion

The RadiForce RX660 was determined to be substantially equivalent to the predicate device due to the following reasons:

- . The stated intended use is substantially the same as that of the predicate device.
- . It was confirmed that the technological characteristics differences from those of the predicate device do not affect the safety or the effectiveness.
- . The bench tests demonstrated that the display characteristics are equivalent to those of the predicate device.