← Product Code [LMD](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMD) · K992352 # ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0 (K992352) _Inteleradiology, Inc. · LMD · Sep 29, 1999 · Radiology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMD/K992352 ## Device Facts - **Applicant:** Inteleradiology, Inc. - **Product Code:** [LMD](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMD.md) - **Decision Date:** Sep 29, 1999 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 892.2020 - **Device Class:** Class 1 - **Review Panel:** Radiology - **Attributes:** Software as a Medical Device ## Indications for Use iTR2000 is a software communications tool intended to be used in the transportation, storage and retrieval of digital medical images for the purpose of off-site review. ## Device Story iTR2000 is a standalone teleradiology software tool for remote access to medical images. It facilitates transmission, storage, and retrieval of digital images from modalities like CT, US, MRI, NM, and digital angiography. It enables web-based viewing via standard browsers or proprietary software. Used by radiologists and referring physicians in clinical settings for off-site review. The system supports JPEG compression for image transfer. It does not control imaging hardware; it acts as a communication layer for legacy or non-PACS equipment. Healthcare providers use the retrieved images to support clinical decision-making. Benefits include remote access to diagnostic studies, facilitating on-call activities and off-site consultations. ## Clinical Evidence Bench testing only. Functional validation included product specification development, coding, debugging, and in-house validation. System performance was verified through the successful transfer of over 1200 complete diagnostic imaging studies. No clinical data provided. ## Technological Characteristics Software-only product; operates on standard PC hardware. Supports JPEG compression (ISO/IEC 10918-1). Connectivity via internet/web browser. Implements standard data communications controls for error detection and correction. Designed for small-matrix imaging modalities. ## Regulatory Identification A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, and interfaces. It may provide simple image review software functionality for medical image processing and manipulation, such as grayscale window and level, zoom and pan, user delineated geometric measurements, compression, or user added image annotations. The device does not perform advanced image processing or complex quantitative functions. This does not include electronic transfer of medical image software functions. ## Predicate Devices - WINRAD Teleradiology System (Line Imaging Systems) - AMICAS Web/Intranet Image Server (AutoCyt Group, Inc.) ## 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}------------------------------------------------ #### INTEL ITR 2000 2400 Lorain Road San Marino, California 91108 - Oan Manhol Callonia - Phone (626) 457-1789 Fax (626) 457-1789 Email: info@inteleradiology.com Website: www.inteleradiology.com N C SEP 2 9 1999 Food and Drug Administration Center for Devices and Radiological Health Document Mail Center (HFZ-401) 9200 Corporate Boulevard Rockville, Maryland 20850 ## 510(k) Summary ## 1. Identification | Date Prepared: | July 11, 1999 | |----------------|-----------------------------------------------------------------------------| | Submitter | inTeleRadiology, Inc.
2400 Lorain Road
San Marino, California 91108 | | Contact | Michael Vincent Klein, M.D.
Phone: (626) 457-1789
Fax: (626) 457-1789 | ## 2. Device Name | Proprietary Name: | iTR2000TM: internet TeleradiologyTM | |-------------------------|--------------------------------------| | Common Name: | Teleradiology Software | | Classification
Name: | System, Digital Image Communications | ## 3. Registration Number: Pending ## 4. Classification | Class: | 2 | |---------------|-----------| | Panel: | Radiology | | Product Code: | LMD | {1}------------------------------------------------ # 510(k) Summary - continued #### 5. Standards | Performance: | None established | |--------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Voluntary: | American College of Radiology Standard for Teleradiology (Revision 35 -
1998; for small matrix systems) | | | ISO/IEC 10918-1 Digital Compression and Coding of Continuous-Tone Still
Images [also known as Joint Photographic Experts Group (JPEG):]
Revision 13. July 1994] | #### 6. Predicate Devices WINRAD Teleradiology System (Line Imaging Systems) AMICAS Web/Intranet Image Server (AutoCyt Group, Inc.) #### 7. Device Description iTR2000™ is a stand-alone software product which may be marketed as a software-only product, as well as for use in conjunction with standard PC hardware, off-the-shelf software or third-party teleradiology/PACS software. iTR2000™ provides short-term remote access to medical images by radiologists, referring physicians and other licensed professionals, utilizing a personal computer or workstation with internet access. Images are securely stored on a internet website for on-demand remote retrieval via the iTR2000™ software, or via a standard web browser without the use of propriety software. The iTR2000™ system employs the latest internet security techniques and meets all current federal medical communications standards including recent proposals from HCFA and HHS. iTR2000™ is primarily intended to allow the transmission, retrieval and review of images produced by imaging equipment otherwise not part of a digital Picture Archive and Communication System (PACS) network or legacy equipment not compatible with ACR/NEMA DICOM 3.0. Conventional film-based images can be optically digitized and stored in a standard image format, such as JPEG. iTR2000™ can also be configured to web-enable third-party DICOM-capable teleradiology/PACS systems in low-volume environments for remote or on-call activities. iTR2000™ is designed for use primarily with small-matrix imaging modalities, such as images produced by Computed Tomography (CT), Ultrasound (US), Magnetic Resonance Imaging (MRI), Nuclear Medicine (NM), digital flourography and digital angiography. The use of images produced by large-matrix imaging systems, such as digitized radiographic films and computed radiography or mammography. requires the use of digitization and viewing equipment which exceed the stated minimum requirements for the standard iTR2000™ system. iTR2000™ does not control the actual image-taking system (i.e. x-ray, MRI, ultrasound or scintography machines). {2}------------------------------------------------ N C iTR2000™ is a software communications tool intended to be used in the transportation, storage and retrieval of digital medical images for the purpose of off-site review. #### 9. Safety and Effectiveness The iTR2000™ software is primarily an image communications software program used to transfer digital image files between personal computers and is utilized only by competent medical professionals. The system has no patient contacting components. The device does not impact the quality of the original acquired image data. It does not require specialized or nonstandard devices of any type. Competent health professionals would reasonably be expected to exercise judgment and professional expertise in the use and interpretation of the transferred image files. Similar to the predicate devices. iTR2000™ can be used with image compression to remove redundant or unimportant information in the original image data. The recommended JPEG image compression libraries and default compression settings are believed to be substantially equivalent to the libraries used in the previously cleared products. #### 9. Testing The safety of this program has been determined through the various stages of software development which included the development of product specifications, coding, testing, debugging, in-house validation and field maintenance. Functional testing including the transfer of diagnostic imaging studies for over 1200 complete studies. Standard data communications controls for error detection and correction are utilized. #### 10. Conclusions iTR2000™ software is a medical device, and it has the same indications for use, the same technological characteristics and the same target population as the legally marketed predicate devices. Any differences between the iTR2000™ software and the predicate devices have no significant influence on safety or efficacy. The iTR2000™ system employs the latest internet security techniques and meets all current federal medical communications standards including recent proposals from HCFA and HHS. No new issues of safety and effectiveness are raised. InTeleRadiology, Inc., believes sufficient information is included to reach a determination of substantial equivalence. We conclude that the iTR2000™ software is as safe and effective as the legally marketed devices and is substantially equivalent to the previously marketed devices (as listed above in Part 6), Michael Vincent Klein. July 11, 1999 July 11, 1996 {3}------------------------------------------------ Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three lines forming its body and wings. The eagle is encircled by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" in a circular arrangement. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 SEP 2 9 1999 Michael Vincent Klein, M.D. CEO Inteleradiology, Inc. 2400 Lorain Road San Marino, CA 91108 Dear Dr. Klein: Re: K992352 ITR2000 Internet Teleradiology Dated: July 11, 1999 Received: July 14, 1999 Product Code: 90 LMD Requlatory Class: I (one) 21 CFR 892.2020 We have reviewed your Section 510(k) notification of intent to market the device referenced above and we 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). 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. Ilsing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either 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 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition. FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. This letter will allow you to begin marketing your device as described in your 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 and additionally 809.10 for in with diagnostic devices), please contact the Office of Compliance at (301) 594-4613. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification"(21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597, or at its internet address "http://www.fda.gov/cdrh/dsma/dsmamain.html". Sincerely yours, CAPT Daniel G. Schultz, M.D. Acting Director, Division of Reproductive, Abdominal, Ear, Nose and Throat, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ 0002 Page 2 of 2 | 510(k) Number (if known): ____ | K992352 | |--------------------------------|---------| |--------------------------------|---------| iTR2000 Device Name: Indications For Use: iTR2000 is a software communications tool intended to be used in the transportation, storage and retrieval of digital medical images for the purpose of off-site review. (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) David G. Syphm (Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices 510(k) Number **Prescription Use** (Per 21 CFR 801.109) OR Over-The-Counter Use_ (Optional Format 1-2-96) --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMD/K992352](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMD/K992352) **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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