← Product Code [EHD](/submissions/DE/subpart-b%E2%80%94diagnostic-devices/EHD) · K972968 # ROTOGRAPH PLUS (K972968) _Chicago X-Ray Systems, Inc. · EHD · Oct 8, 1997 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/EHD/K972968 ## Device Facts - **Applicant:** Chicago X-Ray Systems, Inc. - **Product Code:** [EHD](/submissions/DE/subpart-b%E2%80%94diagnostic-devices/EHD.md) - **Decision Date:** Oct 8, 1997 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.1800 - **Device Class:** Class 2 - **Review Panel:** Dental ## Intended Use The Rotograph Plus as manufactured by Villa Sistemi Medicali S.p.A of Milan, Italy is intended to be used as an extra oral radiological device for the examination of the human dentition and related anatomy as well as craniostatic examinations. They are to be used for Panoramic and Cephalometric Radiology as it is applied to dental diagnosis in dentistry. ## Device Story Rotograph Plus is a dental extra-oral X-ray system used for panoramic and cephalometric imaging. Operated by dental professionals in clinical settings, the device captures radiographic images of human dentition and craniostatic anatomy. It functions as a diagnostic tool to assist clinicians in dental assessment and treatment planning. The system operates under FDA/DHHS radiation-emitting device standards. ## Clinical Evidence No clinical data provided; bench testing and compliance with FDA/DHHS radiation performance standards and international standards (IEC 601.1, 601.2.7) cited. ## Technological Characteristics Extra-oral dental X-ray system. Complies with 21 CFR Subchapter J, IEC 601.1, and IEC 601.2.7 radiation safety standards. Designed for panoramic and cephalometric imaging. ## Regulatory Identification An extraoral source x-ray system is an AC-powered device that produces x-rays and is intended for dental radiographic examination and diagnosis of diseases of the teeth, jaw, and oral structures. The x-ray source (a tube) is located outside the mouth. This generic type of device may include patient and equipment supports and component parts. ## Predicate Devices - Belmont X-Caliber unit ## 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}------------------------------------------------ K9'112768 Image /page/0/Picture/2 description: This image shows a world map. The continents of North America, South America, Europe, Africa, Asia, and Australia are visible. The map is a simple black and white silhouette, with the land masses in black and the oceans in white. chicagox-ray@worldnet.att.net OCT -- 8 1997 510 ( k) SUMMARY FOR Product name: ROTOGRAPH PLUS This product is manufactured by the Villa Sistemi Medicali company of Milan, Italy and is classified as a class II device. It is intended to be used as a dental extra oral x-ray device for the panoramic and cephalometric examination of the human anatomy as it applies to dentistry. This product is manufactured under the guidelines of the FDA/DHHS performance standards as it applies to radiation emitting devices and 21 CFR Subchapter J and the International Standard IEC 601.1 and 601.2.7. This product is substantially equivalent to the Belmont X-Caliber unit as marketed in the United States. The manufacturer further warrants that this device is safe and effective for its intended use. {1}------------------------------------------------ Image /page/1/Picture/0 description: The image shows a seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the border. The seal features a stylized eagle-like bird with three curved lines representing its wings or feathers. The bird is facing right, and the overall design is simple and monochromatic. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 - 8 1997 Re: Al Sosa President Chicago X-Ray System Inc. 219 Mayer Avenue Wheeling, IL 60090 K972968 Rotograph Plus System Software Dated: August 8, 1997 Received: August 11, 1997 Regulatory class: II 21 CFR 872.1800/Procode: 90 EHD Dear Mr. Sosa: 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 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, 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 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (OS) 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 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 vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4613. Additionally, for question 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/dsmamain.html". Sincerely yours. hĩ tiêu Yui Lillian Yin, Ph.D. Director, Division of Reproductive, Abdominal, Ear, Nose and Throat, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## CHICAGO X SYSTEMS IN Image /page/2/Picture/1 description: This image shows a world map. The continents of North America, South America, Europe, Africa, Asia, and Australia are visible. The map is a simple black and white silhouette, with the land masses in black and the oceans in white. 219 Mayer Avenue Wheeling, IL 60090 Pho: 847-459-3889 FAX: 847-459-9214 chicagox-ray@worldnet.att.net Friday, August 08, 1997 510 (K) Number ( if known): Device name: ROTOGRAPH PLUS INDICATIONS FOR USE: The Rotograph Plus as manufactured by Villa Sistemi Medicali S.p.A of Milan, Italy is intended to be used as an extra oral radiological device for the examination of the human dentition and related anatomy as well as craniostatic examinations. They are to be used for Panoramic and Cephalometric Radiology as it is applied to dental diagnosis in dentistry. Concurrence of CDRH, Office of Device Evaluation (ODE) Edward G. Seyson (Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices 510(k) Number **Prescription Use** (Per 21 CFR 801.109) ﻟﻠﺘﻨﺰﻳﻨﺔ --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/EHD/K972968](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/EHD/K972968) **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. If you're preparing [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/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com