NIO 3MP-21

K051901 · Barcoview · LLZ · Aug 17, 2005 · Radiology

Device Facts

• Record ID: K051901
• Device Name: NIO 3MP-21
• Applicant: Barcoview
• Product Code: LLZ · Radiology
• Decision Date: Aug 17, 2005
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.2050
• Device Class: Class 2

Intended Use

The Nio 3MP-21" is intended to be used in displaying and viewing digital images for review by trained medical practitioners. These devices must not be used in primary image diagnosis in mammography.

Device Story

Nio 3MP-21" is a medical display system comprising a 21-inch grayscale LCD (E-3621), a high-resolution display controller board (BarcoMed Nio), and NioWatch software. The system receives digital image data from a PACS workstation; the controller board processes signals via an 8-bit in, 10-bit out lookup table to provide 256 simultaneous shades of gray. NioWatch software enables display calibration, test pattern generation, and optimization for DICOM-compliant viewing. Used in clinical settings by trained medical practitioners for image review; does not perform primary diagnosis for mammography. The system supports landscape or portrait orientations. It does not contact patients or control life-sustaining equipment.

Clinical Evidence

Bench testing only. No clinical data provided.

Technological Characteristics

21-inch grayscale LCD display (E-3621) with 2048x1536 resolution. Includes 10-bit display controller board with 8-bit in/10-bit out lookup table. Features backlight sensor. NioWatch software for calibration and DICOM-compliant viewing. Non-contact device.

Indications for Use

Indicated for display and review of digital medical images by trained medical practitioners. Contraindicated for primary image diagnosis in mammography.

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

• Nio 2MP Medical flat panel display system (K042660)
• MFGD 2320 20-inch 2 Megapixel grayscale display (K033004)

Submission Summary (Full Text)

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K05190L

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

#### 1. Date of preparation

AUG 1 7 2005

July 05, 2005

# 2. Company information

- BarcoView 35 President Kennedypark B-8500 Kortrijk, Belgium Tel. [phone] Fax [phone]
## 3. Contact person

Lieven De Wandel Official correspondent

#### 4. Device information

- Trade name: Nio 3MP-21" ~ �
- Common name: Display system, medical image workstation, and others .
- Classification name: System, Image Processing �
- Classification number: 21 CFR 892.2050 / Procode 90LLZ .

## 5. Predicate device

- Name: Nio 2MP Medical flat panel display system .
- 510(k) number: K042660 V �
- Manufacturer: Barco NV .

## 6. Device description

Nio 3MP-21" is a display system for medical viewing. It consists of 3 components:

E-3621 is a 21" grayscale LCD display. BarcoMed Nio is a fast high-resolution display controller board that plugs into a PACS workstation computer. NioWatch is user-friendly software that allows to optimize the display for DICOM-compliant viewing.

The display system can be a single-head system or multi-head system. In the last case it contains multiple displays and display controller boards.

## 7. Intended use

"The Nio 3MP-21" is intended to be used in displaying and viewing digital images for review by trained medical practitioners. These devices must not be used in primary image diagnosis in mammography.

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# 8. Summary of technological characteristics

The device consists of three components:

- One 3-meqapixel flat panel display (E-3621) .
- . One 10-bit display controller (BarcoMed Nio board)
- . NioWatch software

The flat panel display has a resolution of 2048x1536 pixels. It can be used in landscape and portrait mode.

The display controller board is an ultra-high speed board with an 8-bit in, 10-bit out lookup table, providing 256 simultaneous shades of gray.

The NioWatch software allows to set the display function, display test patterns, calibrate the display and view additional display and display controller information.

Compared to the predicate device, the display from the Nio 3MP-21" system has a different LCD panel with somewhat larger screen size and higher resolution. The other components of the system are the same.

The device does not come into contact with the patient. It does not control any life sustaining devices either.

## 9. Conclusion:

The Barco Nio 3MP-21" is substantially equivalent to the predicate device, Nio 2MP Medical flat panel display system.

The new and predicate devices are substantially equivalent in the areas of technical characteristics, general function, application and intended use.

Any difference between both devices does not affect safety or efficacy.

The 510(k) Pre-Market Notification for the Barco Nio 3MP-21" contains adequate information and data to enable FDA - CDRH to determine substantial equivalence to the predicate device.

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

## 1. Date of preparation

July 05, 2005

# 2. Company information

BarcoView 35 President Kennedypark B-8500 Kortrijk, Belgium Tel. [phone] Fax [phone]

## 3. Contact person

Lieven De Wandel Official correspondent

## 4. Device information

- Trade name: E-3621 .
- Common name: Display system, medical image workstation, and others .
- Classification name: System, Image Processing ●
- Classification number: 21 CFR 892.2050 / Procode 90LLZ .

## 5. Predicate device

- Name: MFGD 2320 20-inch 2 Megapixel grayscale display .
- 510(k) number: K033004 ~ .
- Manufacturer: Barco NV .

## 6. Device description

E-3621 is a 21" grayscale LCD display for medical viewing. It is combined with NioWatch, a userfriendly software that allows to optimize the display for DICOM-compliant viewing.

## 7. Intended use

The E-3621 is intended to be used in displaying and viewing digital images for review by trained medical practitioners. These devices must not be used in primary image diagnosis in mammography.

## 8. Summary of technological characteristics

The flat panel display has a resolution of 2048x1536 pixels. It can be used in landscape on

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portrait mode.

The NioWatch software allows to set the display function, display test patterns, calibrate the display and view additional display information.

Compared to the predicate device, the E-3621 display has a different LCD panel with larger screen size and higher resolution, and contains a backlight sensor instead of a front sensor.

The device does not come into contact with the patient. It does not control any life sustaining devices either.

#### 9. Conclusion:

The Barco E-3621 is substantially equivalent to the predicate device, MFGD 2320 20-inch 2 Megapixel grayscale display.

The new and predicate devices are substantially equivalent in the areas of technical characteristics, general function, application and intended use.

Any difference between both devices does not affect safety or efficacy.

The 510(k) Pre-Market Notification for the Barco E-3621 contains adequate information and data to enable FDA - CDRH to determine substantial equivalence to the predicate device.

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Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

Mr. Lieven De Wandel Official Correspondent Barco-Medical Imaging Systems President Kennedypark 35 B-8500 Kortrijk BELGIUM

Re: K051901

AUG 1 7 2005

Trade/Device Name: Nio 3MP-21 Medical Flat Panel Display System and E-3621 Medical Flat Panel Display Regulation Number: 21 CFR 892.2050 Regulation Name: Picture archiving and communications system

Regulatory Class: II Product Code: LLZ Dated: July 5, 2005 Received: July 13, 2005

Dear Mr. De Wandel:

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 (Premarket Approval), it may be subject to such 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); good manufacturing practice requirements as set forth in the quality systems (OS) 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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This letter will allow you to begin marketing your device as described in your Section 510(k) I ms letter will anow you to organization of substantial equivalence of your device to a legally prematics notifiedding - results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please rr you don't if you of Compliance at one of the following numbers, based on the regulation number at the top of this letter:

| 21 CFR 876.xxxx | (Gastroenterology/Renal/Urology) | 240-276-0115 |
|-----------------|----------------------------------|--------------|
| 21 CFR 884.xxxx | (Obstetrics/Gynecology) | 240-276-0115 |
| 21 CFR 892.xxxx | (Radiology) | 240-276-0120 |
| Other | | 240-276-0100 |

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). You may obtain other general information on your responsibilities under the Act from the 001:57). I od may overnmentional and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.

Sincerely yours,

Nancy C. Brogdon

Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# INDICATIONS FOR USE

10(k) Number (if known): ----------------

Device Name: E-3621

Indications for Use:

"The E-3621 is intended to be used in displaying and viewing digital images for review by trained medical practitioners. These devices must not be used in primary image diagnosis in mammography.

Prescription Use XX (Part 21 CFR 801 Subpart D) AND/OR (21 CFR 801 Subpart C)

Over-The-Counter Use

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Nancy C bragdon

(Division Sign Off Division of Reproduct and Radiological Devices 510(k) Number