← Product Code [JAK](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAK) · K970999 # SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR (K970999) _Sony Medical Systems · JAK · May 20, 1997 · Radiology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAK/K970999 ## Device Facts - **Applicant:** Sony Medical Systems - **Product Code:** [JAK](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAK.md) - **Decision Date:** May 20, 1997 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 892.1750 - **Device Class:** Class 2 - **Review Panel:** Radiology ## Indications for Use The Sony PGM-100P1MD Trinitron® Color Graphic Monitor is intended for use in patient monitoring applications to display multi-parameter data in graphic format. The Sony PGM-100P1MD can be used in hospital settings such as the intensive care unit, central station, and nurse station. Applications include the display of data from electrocardiographs, blood pressure and pulse measurement systems, and computed tomography and other imaging systems. ## Device Story Sony PGM-100P1MD is a general-purpose computer monitor modified for medical patient monitoring. Device accepts standard video signals from PC-compatible computers and medical imaging/monitoring systems. It displays multi-parameter data (ECG, blood pressure, pulse, CT images) in graphic format. Used in hospital environments like ICUs and nurse stations; operated by clinical staff. Output allows clinicians to visualize patient data for monitoring and diagnostic decision-making. Benefits include high-resolution graphical display of patient information. ## Clinical Evidence No clinical data. Bench testing only. ## Technological Characteristics Trinitron® color graphic monitor; PC-compatible; accepts standard video signals; higher resolution than predicate monitors. Standalone display device. ## Regulatory Identification A computed tomography x-ray system is a diagnostic x-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from the same axial plane taken at different angles. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. ## Predicate Devices - Sony Trinitron Color Video Monitor PVM-1343MD ([K885042](/device/K885042.md)) - Electrohome M1544/1744 High Resolution Monochrome Monitors - Siemens Sirecust 1481T Digital Telemetry System ([K900319](/device/K900319.md)) ## 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} K970999 MAY 20 1997 510(k) Summary for Sony PGM-100P1MD Trinitron® Color Graphic Monitor 1. Applicant: Sony Medical Systems Division Sony Electronics Inc. 3 Paragon Drive Montvale, NJ 07645 Contact Person: Anthony John Kefalos Telephone: 201-358-4330 Date Prepared: March 18, 1997 2. Device Name Proprietary Name: Sony PGM-100P1MD Trinitron® Color Graphic Monitor Common/Usual Name: Color Graphic Monitor Classification Name: Accessory to Medical Imaging, Monitoring and Diagnostic Devices Classification Status: Class II 3. Predicate Devices - Sony Trinitron Color Video Monitor PVM-1343MD Sony Medical Systems Division K885042 - Electrohome M1544/1744 High Resolution Monochrome Monitors Electrohome Limited - Siemens Sirecust 1481T Digital Telemetry System (includes the Sony Trinitron® Character Display CPD-1304 as the monitor component) Siemens Medical Electronics, Inc. K900319 Sony PGM-100P1MD Monitor 510(k) 3/18/97 Page D-1 {1} # 4. Device Description The Sony PGM-100P1MD Trinitron® Color Graphic Monitor is a general purpose computer monitor which has been modified for use in medical settings for patient monitoring applications. It will display images received from a computer system and is designed for use with PC-compatible computers. # 5. Intended Use The Sony PGM-100P1MD Trinitron® Color Graphic Monitor is intended for use in patient monitoring applications to display multi-parameter data in graphic format. # 6. Technological Characteristics The Sony PGM-100P1MD Trinitron® Color Graphic Monitor is intended as an addition to the Sony video monitor product line and has the same general purposes and function as the predicate devices identified above. All of the devices accept standard video signals produced by a wide range of equipment. The primary difference between the Sony PGM-100P1MD and the predicate devices is the higher resolution that it provides for use in graphical display. Sony PGM-100P1MD Monitor 510(k) 3/18/97 Page D-2 {2} DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 MAY 20 1997 Cynthia A. Sinclair Sony Medical Systems C/O Medical Device Consult, Inc. 49 Plain Street North Attleboro, MA 02760 Re: K970999 Sony PGM-100P1MD Trinitron® Color Graphic Monitor Dated: March 18, 1997 Received: March 19, 1997 Regulatory class: II 21 CFR 892.1750/Procode: 90 JAK Dear Ms. Sinclair: 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, 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 895. A substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP 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 vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4591 for Radiology devices, or 594-4613 for Ear, Nose and Throat devices. 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/dsmamain.html". Sincerely yours, 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 {3} 510(k) Number (if known): K970999 Device Name: Sony PGM-100P1MD Trinitron® Color Graphic Monitor Indications For Use: The Sony PGM-100P1MD Trinitron® Color Graphic Monitor is intended for use in patient monitoring applications to display multi-parameter data in graphic format. The Sony PGM-100P1MD can be used in hospital settings such as the intensive care unit, central station, and nurse station. Applications include the display of data from electrocardiographs, blood pressure and pulse measurement systems, and computed tomography and other imaging systems. (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) David C. Lyman (Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices 510(k) Number K970999 Prescription Use ☑ (Per 21 CFR 801.109) OR Over-The-Counter Use ☐ (Optional Format 1-2-96) Sony PGM-100P1MD Monitor 510(k) 3/18/97 --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAK/K970999](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAK/K970999) **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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