PLANAR DOME EX SERIES DIGITAL FLAT-PANEL DISPLAY SYSTEM, MODEL E4C COLOR

K060136 · Planar Systems, Inc. · LLZ · Jan 31, 2006 · Radiology

Device Facts

• Record ID: K060136
• Device Name: PLANAR DOME EX SERIES DIGITAL FLAT-PANEL DISPLAY SYSTEM, MODEL E4C COLOR
• Applicant: Planar Systems, Inc.
• Product Code: LLZ · Radiology
• Decision Date: Jan 31, 2006
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.2050
• Device Class: Class 2
• Attributes: 3rd-Party Reviewed

Indications for Use

The Planar DOME DIGITAL FLAT-PANEL DISPLAY SYSTEM™, Model E4c™ is intended to be used in displaying and viewing medical images for review and analysis by trained medical practitioners. This device must not be used in primary image diagnosis in mammography.

Device Story

Planar DOME EX E4c is a high-resolution LCD monitor system for medical image display. System comprises LCD monitor and high-resolution graphic control board installed in PACS workstation. Cxtra software optimizes display for DICOM-compliant viewing. Used in clinical settings by trained medical practitioners for image review and analysis. Output allows clinicians to visualize diagnostic images; supports clinical decision-making by providing standardized, high-fidelity image presentation. Benefits include improved image clarity and consistency for diagnostic review.

Clinical Evidence

Bench testing only. Device validated for intended use against safety standards and DICOM PS3.14 compliance. Hazard analysis classified potential hazards as minor.

Technological Characteristics

Flat-panel LCD monitor; high-resolution graphic control board; DICOM PS3.14 compliant; software-based display optimization (Cxtra).

Indications for Use

Indicated for display and review of 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

• BARCO NV, CORONIS 3MP MEDICAL FLAT PANEL DISPLAY SYSTEM (K013922)
• Planar DOME CX DIGITAL FLAT-PANEL DISPLAY SYSTEM, Models C3 Color and C3 Gray (K032638)

Submission Summary (Full Text)

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K060136

1195 NW Compton Drive, Beaverton, OR 97006-1992, USA Phone: [phone] Fax: [phone] www.planar.com PLANAR

JAN 3 ] 2006

## 510(k) SUMMARY OF SAFETY AND EFFECTIVENESS

| Summary Date: | 8 December 2005 |
|-------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| 21 CFR 807.92(a)(1)<br>Submitter's Information: | Mr. Craig Harshman<br>Planar Systems, Inc.<br>1195 NW Compton Drive<br>Beaverton, OR 97006-1992<br>[phone] (Phone)<br>[phone] (fax)<br>[e-mail] (Email) |
| 21 CFR 807.92(a)(2)<br>Device Trade Name | PLANAR DOME EX SERIES DIGITAL FLAT-PANEL DISPLAY<br>SYSTEM ^TM , Model E4c Color ^TM |
| Device common Name: | SYSTEM, IMAGE PROCESSING, RADIOLOGICAL |
| Device Classification Name: | 892.2050 Picture archiving and communications system |
| Classification Product Code | LLZ |
| Establishment Registration<br>Number | 1226517 |
| Device Class: | Class II |
| Classification Advisory<br>Committee: | Radiology |
| 21 CFR 807.92(a)(3)<br>Predicate Devices: | The predicate devices:<br>510(k) Number: K013922<br>Decision Date: 01/28/2002<br>BARCO NV, CORONIS 3MP MEDICAL FLAT PANEL DISPLAY<br>SYSTEM ^TM<br>And<br>510(k) Number: K032638<br>Decision Date: 09/11/2003<br>Planar DOME CX ^TM DIGITAL FLAT-PANEL DISPLAY SYSTEM ^TM ,<br>Models C3 Color ^TM and C3 Gray ^TM . |
| 21 CFR 807.92(a)(4)<br>Device Description: | The Planar DOME EX ^TM DIGITAL FLAT-PANEL DISPLAY SYSTEM ^TM ,<br>Models E4c Color ^TM is a flat panel hi-resolution LCD monitor systems<br>for displaying medical images. The system consists of a LCD monitor<br>and a high-resolution graphic control board that connects to a PACS<br>workstation for image display. The controller board is installed into the<br>PACS workstation computer or other computer system used to display<br>PACS medical images. Cxtra is user-friendly software that purpose is<br>to optimize the display for DICOM-compliant viewing. |
| 21 CFR 807.92(a)(5)<br>Intended Use: | The Planar DOME DIGITAL FLAT-PANEL DISPLAY SYSTEM ^TM ,<br>Model E4c ^TM is intended to be used in displaying and viewing medical<br>images for review and analysis by trained medical practitioners. This<br>device must not be used in primary image diagnosis in mammography. |

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## 21 CFR 807.92(a)(6) Substantial Equivalence:

The Planar DOME EX™ DIGITAL FLAT-PANEL DISPLAY SYSTEM™. Models E4c Color™ is substantially equivalent to the BARCO NV, CORONIS 3MP MEDICAL FLAT PANEL DISPLAY SYSTEM™ (K013922) and the Planar DOME CX™ DIGITAL FLAT-PANEL DISPLAY SYSTEM™, Models C3 Color™ and C3 Gray™ (K032638) in that:

- . The subsection of the system are similar in that they each consist of:
- o Display Monitor
- Graphic controller card installed in a PACS or PC. o
- Software 0
- . Intended use is same
- Performance attributes are similar .
- Follow DICOM PS3.14 "Grayscale Standard Display Function" .

This 510(k) Pre-Market Notification for the Planar DOME EX™ DIGITAL FLAT-PANEL DISPLAY SYSTEM™. Models E4c Color™ contain adequate information and data to enable FDA - CDRH to determine substantial equivalence to the predicate device.

The Planar DOME EX™ DIGITAL FLAT-PANEL DISPLAY SYSTEM™, Models E4c Color™ has been tested to various Standards and was validated for its intended use.

The Planar DOME EX™ DIGITAL FLAT-PANEL DISPLAY SYSTEM™. Models E4c Color™ will be manufactured by in accordance with voluntary and safety standards

This submission contains the results of a hazard analysis and the potential hazards have been classified as Minor

21 CFR 807.92(b) Conclusions and Statements:

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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three stripes representing the three levels of government: federal, state, and local. The eagle is encircled by the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" in a circular arrangement.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

JAN 3 1 2006

Planar Systems, Inc. % Ms. Melissa J. DeGuia Project Engineer Underwriters Laboratories, Inc. 2600 NW Lake Road CAMAS WA 98607

Re: K060136

Trade/Device Name: DOME EX™ Digital Flat-Panel Display System™, Models E4cTM Regulation Number: 21 CFR 892.2050 Regulation Name: Picture archiving and communications system Regulatory Class: II Product Code: LLZ Dated: January 18, 2006 Received: January 19, 2006

Dear Ms. DeGuia:

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 (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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This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device 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 contact the Office 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 Division of Small Manufacturers, International 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.

Sincercly yours.

Nancy C. Brigdon

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

510(k) Number (if known): K 060 136

Device Name:

DOME EX™ DIGITAL FLAT-PANEL DISPLAY SYSTEM™, Models E4c™ .

Indications for Use:

The Planar DOME DIGITAL FLAT-PANEL DISPLAY SYSTEM™, Model E4c™ is intended to be used in displaying and viewing medical images for review and analysis by trained medical practitioners.

This device must not be used in primary image diagnosis in mammography.

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

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

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

Concurrence of CDRH, Office of Device Evaluation (ODE)

Page 1 of -1

(Posted November 13, 2003)

Nancy Brogdon

(Division Sign-Off) Division of Reproductive, A and Radiological Devices 510(k) Number _