← Product Code [KPR](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/KPR) · K103448 # BRIVO XR385 (K103448) _Ge Medical Systems, LLC · KPR · Aug 12, 2011 · Radiology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/KPR/K103448 ## Device Facts - **Applicant:** Ge Medical Systems, LLC - **Product Code:** [KPR](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/KPR.md) - **Decision Date:** Aug 12, 2011 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 892.1680 - **Device Class:** Class 2 - **Review Panel:** Radiology - **Attributes:** Pediatric ## Intended Use The Brivo XR385 Digital X-Ray System is intended for use on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position. This device is not intended for mammographic applications. ## Device Story Brivo XR385 is a stationary digital diagnostic radiographic system; captures radiographic images using an X-ray tube and digital detector. System includes integrated tube stand, patient support table with floating top, under-table high-voltage generator, manual beam-limiting device, and wall stand. Acquisition and review workstation performs image post-processing, short-term storage, and in-room viewing. Images transferred via DICOM network for printing, long-term archiving, and review. Operated by healthcare professionals in clinical settings. Provides high-quality digital radiographic images to assist in diagnostic decision-making. ## Clinical Evidence No clinical data. Substantial equivalence supported by bench testing, module verification, system integration testing, performance verification, safety testing, and simulated use validation. ## Technological Characteristics Stationary X-ray system; dual focal spot X-ray tube; GdOS scintillator digital detector; acquisition and review workstation. Connectivity via DICOM network. System includes integrated tube stand, floating table top, and under-table high-voltage generator. ## Regulatory 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 - Silhouette VR ([K982955](/device/K982955.md)) - GE Tethered Portable Digital Radiographic Detector ([K041922](/device/K041922.md)) - Canon digital radiography CXDI-50G ([K031447](/device/K031447.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}------------------------------------------------ K103448 Image /page/0/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The logo is black and white. AUG 1 2 2011 # GE Healthcare 510(k) Premarket Notification Submission Section 5: 510(k) Summary Brivo XR385 # 510(k) Summary 5-2 {1}------------------------------------------------ Image /page/1/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The logo is black and white. # 510(k) Premarket Notification Submission : ### 510(k) Summary | In accordance with 21 CFR 807.92 the following summary of information is provided: | | |------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Date: | November 19, 2010 | | Submitter: | GE Healthcare, (GE MEDICAL SYSTEMS, LLC)
3000 N. Grandview blvd. W-709 | | Primary Contact Person: | John L. Schmidt
Regulatory Affairs Leader-X-Ray
GE Healthcare, (GE MEDICAL SYSTEMS, LLC)
TEL: (262) 548-4964
FAX: (262) 548-2721
e-mail: John.L.Schmidt@ge.com | | Secondary Contact Person: | David Blonski
Regulatory Affairs Director
GE Healthcare, (GE MEDICAL SYSTEMS, LLC)
3000 N. Grandview blvd. (W-709)
262 513-4072
548-2721
e-mail: David.Blonski@ge.com | | Device: Trade Name: | Brivo XR385 | | Common/Usual Name: | Digital Diagnostic Radiographic System | | Classification Names: | Stationary X-Ray System (21CFR § 892.1680) and solid state x-
ray imager (21CFR § 892.1650) | | Product Code: | KPR and MQB | | Predicate Device(s): | Stationary x-ray system MODEL: Silhouette VR (K982955)
GE Tethered Portable Digital Radiographic Detector (K041922)
Canon digital radiography CXDI-50G (K031447) | | Device Description: | The Brivo XR385 Digital Diagnostic Radiographic system
provides state of the art image quality, image manipulation,
operator control, dose reporting and system maintenance. These
features make this system easy to use and reliable while
providing high quality radiographic images in a digital
environment. The Brivo XR385 system configuration includes an
integrated tube stand and patient support table with a floating
table top, under-the-table high-voltage generator and power | {2}------------------------------------------------ Image /page/2/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters "G" and "E" intertwined within a circular border. The letters are stylized with curved lines and flourishes, giving the logo a distinctive and recognizable appearance. ray tube, a manual beam limiting device, a wall stand and a digital detector that captures radiographic images in digital form. The system also includes an acquisition and review workstation for image post-processing, short-term storage, and quick in-room viewing of images. Images may be transferred manually or automatically via a DICOM network for printing, long-term storage archive, and detailed review. The Brivo XR385 Digital X-Ray System is intended for use on Intended Use: both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position. This device is not intended for mammographic applications. {3}------------------------------------------------ Image /page/3/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circle. The letters and the circle are in black, contrasting with the white background. The Brivo XR385 Digital Diagnostic Radiographic system Technology: employs the same construction of Silhouette VR Radiographic system: an integrated tube stand and patient support table with a floating table top, under-the-table high-voltage generator and power distribution unit, an X-ray tube assembly with dual focal spot X-ray tube, a manual beam limiting device, and a wall stand. The Brivo XR385 also employs GE's patented digital detector that captures radiographic images in digital form. The digital detector design is the same as the GE Tethered Portable Digital Radiographic detector (also referred to as Trad) with the exception of the scintillator material changing from Csl to GdOS as is in the Canon digital detector CXDI-50G. The system also includes an acquisition and review workstation for image post-processing, short-term storage, and quick in-room viewing of images. Determination of Summary of Non-Clinical Tests: Substantial Equivalence: The Brivo XR385 and its applications comply with voluntary standards and related FDA guidance as detailed in Section 9, 17 and 12 of this premarket submission. The following quality assurance measures were applied to the development of the system: Risk Analysis Requirements Reviews Design Reviews Testing on unit level (Module verification) Integration testing (System verification) Performance testing (Verification) Safety testing (Verification) Simulated use testing (Validation) Summary of Clinical Tests: The subject of this premarket submission, Brivo XR385, did not require clinical studies to support substantial equivalence. After analyzing standards testing and bench data, it is the Conclusion: {4}------------------------------------------------ Image /page/4/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The letters and the border are solid black, contrasting with the white background. conclusion of GE Healthcare that the Brivo XR385 is substantially equivalent to other marketed devices with similar indications for use and meeting the same standards. {5}------------------------------------------------ Image /page/5/Picture/0 description: The image shows a logo for the Department of Health & Human Services. The logo features a stylized eagle with three curved lines representing its body and wings. The text "DEPARTMENT OF HEALTH &" is visible, along with the word "SERVICES" vertically oriented along the left side of the logo. #### DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Room - WO66-G609 Silver Spring, MD 20993-0002 Mr. John L. Schmidt Regulatory Affairs Leader-X-Ray GE Healthcare 3000 N. Grandview Blvd. WAUKESHA WI 53188 AUG 1 2 2011 Re: K103448 Trade/Device Name: Brivo XR385 Regulation Number: 21 CFR 892.1680 Regulation Name: Stationary x-ray system Regulatory Class: II Product Code: KPR Dated: June 30, 2011 Received: July 1, 2011 Dear Mr. Schmidt: 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. ff 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 of {6}------------------------------------------------ Page 2 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 809), please contact the Office of In Viro Diagnostic Device Evaluation and Safety at (301) 796-5450. 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 Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely Yours. Mary Patil. Mary S. Pastel, Sc.D. Director Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health Enclosure {7}------------------------------------------------ Image /page/7/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circle. The logo is black and white. # Indications for Use 510(k) Number (if known): N/A Device Name: Brivo XR385 Indications for Use: The Brivo XR385 Digital X-Ray System is intended for use on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position. This device is not intended for mammographic applications. Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use_ (Part 21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD) Marp Patel Division Sigd-Off Office of In Vitro Diagnostic Device **Evaluation and Safety** 510(k) K103448 --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/KPR/K103448](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/KPR/K103448) **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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