DRAD-3000E, RADREX-I

K073165 · Toshiba America Medical Systems, In.C · MQB · Nov 16, 2007 · Radiology

Device Facts

• Record ID: K073165
• Device Name: DRAD-3000E, RADREX-I
• Applicant: Toshiba America Medical Systems, In.C
• Product Code: MQB · Radiology
• Decision Date: Nov 16, 2007
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.1680
• Device Class: Class 2
• Attributes: 3rd-Party Reviewed

Intended Use

This system is intended for use as a general radiography device for the head, chest, abdomen, spine, neck and limbs. This system is used for image acquisition, image display, and the transmission/output of images to external devices. Excluded indications include mammography, fluoroscopy and angiography.

Device Story

RADREX-i is a general-purpose digital radiography system; utilizes solid-state x-ray imagers (SSXI) to convert x-rays directly into electrical signals. System includes PC-based console for worklist management, image processing, storage, export, and printing; configurable with table, vertical wall unit, and up to two x-ray tubes. Operated by clinical staff in radiology settings. System transforms raw x-ray input into digital images displayed on LCD monitors or printed. Provides diagnostic images to assist clinicians in evaluating anatomy; benefits patients through rapid digital image acquisition and reduced processing time compared to traditional film-based systems.

Clinical Evidence

Bench testing only. The device conforms to Federal Diagnostic X-ray Equipment Standards (21 CFR 1020) and medical device safety standards including IEC 60601-1, IEC 60601-2-32, and IEC 60601-2-28.

Technological Characteristics

General-purpose stationary x-ray system; utilizes solid-state x-ray imagers (SSXI) for direct conversion of x-rays to digital signals. PC-based console for image processing and management. Configurable with table/wall stand and dual x-ray tubes. Complies with 21 CFR 1020, IEC 60601-1, IEC 60601-2-32, and IEC 60601-2-28.

Indications for Use

Indicated for general radiography of head, neck, spine, chest, abdomen, and limbs in patients requiring digital x-ray imaging. Excludes mammography, fluoroscopy, and angiography.

Regulatory Classification

Identification

A stationary x-ray system is a permanently installed diagnostic system intended to generate and control x-rays for examination of various anatomical regions. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

Special Controls

*Classification.* Class II (special controls). A radiographic contrast tray or radiology diagnostic kit intended for use with a stationary x-ray system only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.

Predicate Devices

• Philips Medical Systems Bucky Vision (Digital Diagnost) (K982795)

Submission Summary (Full Text)

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K073/65
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## Toshiba America Medical Systems, Inc. 510(k) Pre-market Notification; DRAD-3000E, RADREX-i

# 510(k) Summary

| Date: | October 30, 2007 |
|---------------------------------------|--------------------------------------------------------------------------------------------------------|
| Submitter's Name: | Toshiba America Medical Systems, Inc. |
| Submitter's Address: | P.O. Box 2068, 2441 Michelle Drive,<br>Tustin, CA 92781-2068<br>NOV 16 2007 |
| Submitter's Contact: | Paul Biggins, Director Regulatory Affairs<br>[phone] |
| Establishment Registration<br>Number: | 2020563 |
| Device Proprietary Name: | DRAD-3000E, RADREX-i |
| Common Name: | Solid State X-ray Imager (Flat Panel/Digital Imager)<br>[Fed. Reg. No. 892.1650, Pro. Code: 90MQB/KPR] |
| Regulatory Class: | II (per 21 CFR 892.1650) |
| Performance Standard: | 21 CFR Subchapter J,<br>Federal Diagnostic X-ray Equipment Standard |
| Predicate Device(s): | Philips Medical Systems Bucky Vision (Digital Diagnost)<br>510(k) Control Number: K982795 |
| Reason For Submission | New device |

### Description of this Device:

The RADREX-I is a general purpose x-ray system that employs Solid State Imager(s), SSXI, which converts x-rays directly into electrical signals which can, after appropriate processing be displayed on LCD monitors or printed to a medical grade image printer. The system console is a PC based device that allows for work list management, image storage, image processing, image exporting and image printing. The system may be equipped with a table and/or vertical wall unit and is configurable with up to two x-ray tubes.

### Summary of Intended Uses:

This system is intended for use as a general radiography device for the head, chest, abdomen, spine, neck and limbs. This system is used for image acquisition, image display, and the transmission/output of images to external devices. Excluded indications include mammography, fluoroscopy and angiography.

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K.C. 73/165

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## Toshiba America Medical Systems, Inc. 510(k) Pre-market Notification; DRAD-3000E, RADREX-i

#### Technological Characteristics:

This device employs similar materials and processes as found in the predicate device. The device produces ionizing radiation that is employed to generate radiographic images of the anatomy.

### Safety and Effectiveness Concerns:

This device is designed and manufactured under the Quality System Regulations as outlined in 21 CFR § 820. All requirements of the Federal Diagnostic Equipment Standard, as outlined in 21 CFR § 1020,that apply to this device, will be met and reported via an initial report. Additionally this system is in conformance with the applicable parts of the IEC 60601-1 {applicable portions}; IEC 60601-2-32, and IEC 60601-2-28. - Medical Device Safety standards.

#### Substantial Equivalence:

The RADREX-I is of comparable type and substantially equivalent to:

Philips Digital Diagnost; k982795

Therefore the RADREX-I complies with the same or equivalent standards and has the same intended use as the predicate device.

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Image /page/2/Picture/0 description: The image shows the logo for the Department of Health & Human Services. The logo consists of two parts: a symbol on the left and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES" on the right. The symbol is a stylized representation of a human figure, and the text is written in a clear, sans-serif font.

Public Health Service

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

Toshiba America Medical Systems, Inc. % Mr. Mark Job Responsible Third Party Official Regulatory Technology Services LLC 1394 25th Street NW BUFFALO MN 55313

Re: K073165

Trade/Device Name: DRAD-3000E; RADREX-i Regulation Number: 21 CFR 892.1680 Regulation Name: Stationary x-ray system Regulatory Class: II Product Code: MOB Dated: November 8, 2007 Received: November 9, 2007

AUG 2 3 2013

Dear Mr. Job:

This letter corrects our substantially equivalent letter of November 16, 2007.

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 class II (Special Controls), it may be subject to such additional controls. Existing major regulations affecting your device can be found in Title 21, Code of Federal Regulations (CFR), Parts 800 to 895. 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 Parts 801 and 809); medical device reporting (reporting of

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medical device-related adverse events) (21 CFR 803); and good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820). 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 Parts 801 and 11 you dosire spoolite darroot 101 your word Diagnostic Device Evaluation and Safety at [phone]. 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 Totallay 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.

Sincerely Yours,

Janine M. Morris

Acting Director Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health

Enclosure

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# Indications for Use

510(k) Number (if known): K073165

DRAD-3000E; RADREX-i Device Name:

Indications for Use:

This device is indicated as a general radiography device. It is capable of providing digital images of the head, neck, spine, chest abdomen and limbs by converting x-rays to digital images. Excluded indications include mammography, fluoroscopy and angiography studies.

Prescription Use
(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 IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

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Hogur Moly
Division Sign-Off

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