Who is the manufacturer of Wireless Digital Flat Panel Detector?

Iray Technology Taicang , Ltd. filed the 510(k) submission for Wireless Digital Flat Panel Detector (K182551).

What is the FDA product code for Wireless Digital Flat Panel Detector?

MQB. It is classified under 21 CFR 892.1680 as a Class 2 device in the Radiology panel.

What is the regulatory pathway for Wireless Digital Flat Panel Detector?

510(k) clearance (submission type: Traditional).

What are the predicate devices for Wireless Digital Flat Panel Detector?

Wireless Digital Flat Panel Detector Mars1417V-PSI (K161730).

Who can help prepare an FDA 510(k) submission like Wireless Digital Flat Panel Detector?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Wireless Digital Flat Panel Detector

K182551 · Iray Technology Taicang , Ltd. · MQB · Oct 17, 2018 · Radiology

Device Facts

Record ID	K182551
Device Name	Wireless Digital Flat Panel Detector
Applicant	Iray Technology Taicang , Ltd.
Product Code	MQB · Radiology
Decision Date	Oct 17, 2018
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 892.1680
Device Class	Class 2

Intended Use

Mars1417XF-CSI Wireless Digital Flat Panel Detector is indicated for digital imaging solution designed for providing general radiographic diagnosis of human anatomy. It is intended to replace radiographic film/screen systems in all general-purpose diagnostic procedures. This device is not intended for mammography or dental applications.

Device Story

Wireless digital flat panel detector; captures X-ray radiation to produce digital images for general radiography. Device uses CsI scintillator to convert X-rays to visible photons; TFT/PD sensor array converts photons to electron signals. Detector integrates with DR system software via SDK/API. Used in clinical settings by healthcare professionals to replace film/screen systems. Output is a digital image displayed on a PC for diagnostic review. Benefits include rapid image acquisition and digitalization of medical X-ray imaging. Operates via wireless communication (IEEE 802.11a/b/g/n) or wired connection. Includes AED trigger module to detect X-ray exposure start/end for automated image acquisition.

Clinical Evidence

Bench testing only; no clinical trials on human subjects. Performance validated via non-clinical studies including DQE, MTF, sensitivity linearity, lag, and noise power spectrum. A concurrence study of 30 phantom images compared the subject device to the predicate (K161730), showing no significant difference in image quality.

Technological Characteristics

Wireless digital flat panel detector; active area 35.04cm x 42.54cm. Scintillator: CsI. Sensor: TFT/PD array. ADC: 16-bit. Connectivity: Wireless IEEE 802.11a/b/g/n (2.4/5 GHz). Housing: Carbon fiber plate. Cooling: Air. Software: SDK-based integration. Biocompatibility: ISO 10993-1 compliant. Electrical/EMC: IEC 60601-1, IEC 60601-1-2.

Indications for Use

Indicated for digital radiographic diagnosis of human anatomy in general-purpose diagnostic procedures. Not for mammography or dental applications. Suitable for patients requiring conventional digital X-ray imaging.

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

Wireless Digital Flat Panel Detector Mars1417V-PSI (K161730)

Related Devices

K182550 — Wireless Digital Flat Panel Detector · Iray Technology Taicang , Ltd. · Oct 17, 2018
K201004 — Wireless Digital Flat Panel Detector Model Name Mars1417V-TSI, Wireless Digital Flat Panel Detector Model Name Mano4336W · Iray Technology Taicang , Ltd. · May 1, 2020
K183713 — Wireless Digital Flat Detector · Iray Technology Taicang , Ltd. · Jan 9, 2019
K213646 — Focus HD 35 Detector · Iray Technology Taicang , Ltd. · Mar 29, 2022
K201043 — Wireless Digital Flat Panel Detector (Model: Mars1717V-VSI, Mano4343W) · Iray Technology Taicang , Ltd. · May 12, 2020

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue. iRay Technology Taicang Ltd. Meng Li Registration and Regulatory Affairs Engineer No. 33 Xinggang Rd., Taicang Port Economic & Technological Development Zone TAICANG, JIANGSU 215434 CN Re: K182551 Trade/Device Name: Wireless Digital Flat Panel Detector Mars 1417XF-CSI Regulation Number: 21 CFR 892.1680 Regulation Name: Stationary x-ray system Regulatory Class: Class II Product Code: MQB Dated: September 13, 2018 Received: September 17, 2018 Dear Meng Li: 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 mav, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be avare that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. October 17, 2018 If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. 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 {1}------------------------------------------------ requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/CombinationProducts/GuidanceRegulatoryInformation/ucm597488.html; good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. 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 comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (http://www.fda.gov/DICE) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely. Michael D. O'Hara For Robert A. Ochs, Ph.D. Director Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration ### Indications for Use 510(k) Number (if known) K182551 Device Name Wireless Digital Flat Panel Detector #### Indications for Use (Describe) Mars1417XF-CSI Wireless Digital Flat Panel Detector is indicated for digital imaging solution designed for providing general radiographic diagnosis of human anatomy. It is intended to replace radiographic film/screen systems in all general-purpose diagnostic procedures. This device is not intended for mammography or dental applications. | | ☑ Prescription Use (Part 21 CFR 801 Subpart D) | | ☐ Over-The-Counter Use (21 CFR 801 Subpart C) | |---------------------------------------------------|-------------------------------------------------------------------------------------------------|---------------------------------------------------|-----------------------------------------------| |---------------------------------------------------|-------------------------------------------------------------------------------------------------|---------------------------------------------------|-----------------------------------------------| **CONTINUE ON A SEPARATE PAGE IF NEEDED.** This section applies only to requirements of the Paperwork Reduction Act of 1995. ***DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*** The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." Type of Use (Select one or both, as applicable) Form Approved: OMB No. 0910-0120 Expiration Date: 06/30/2020 See PRA Statement below. {3}------------------------------------------------ # 510 (k) SUMMARY OF SAFETY AND EFFECTIVENESS (As Required by 21 CFR 807.92) ## 1. Date Prepared [21 CFR 807.92(a)(1)] August 1st, 2018 ### 2. Submitter;s Information [21 CFR 807.92(a)(1)] | Company Name: | iRay Technology Taicang Ltd. | |------------------|-------------------------------------------------------| | Company Address: | No.33 Xinggang Road, Taicang Port Economic and | | | Technological Development Zone, Jiangsu, China 215434 | | Contact Person: | Meng Li | | Phone: | 0512-53690872 | | Fax: | 0512-53690872 | | Email: | meng.li@iraychina.com | ### 3. Trade Name, Common Name, Classification [21 CFR 807.92(a)(2)] | Trade Name: | Wireless Digital Flat Panel Detector | |----------------------|--------------------------------------| | Common Name: | Solid State X-Ray Imager | | Model Name: | Mars1417XF-CSI | | Classification Name: | Stationary X-Ray System | | Product Code: | MQB | | Regulation Number: | 21 CFR 892.1680 | | Device Class: | Class II | ### 4. Identification of Predicate Devices(s) [21 CFR 807.92(a)(3)[ The identification predicates within this submission are as follows: iRay Technology Co.,Ltd. Manufacturer: # 2 of 9 {4}------------------------------------------------ ## iRay Technology Taicang Ltd. | Trade Name: | Wireless Digital Flat Panel Detector | |----------------------|--------------------------------------| | Model Name: | Mars1417V-PSI | | Product Code: | MQB | | Classification Name: | Stationary X-Ray System | | FDA 510 (k) #: | K161730 | #### 5. Description of the Device [21 CFR 807.92(a)(4)] Mars1417XF-CSI Wireless Digital Flat Panel Detector is a kind of wireless digital flat panel detector. It supports the single frame mode, with the key component of TFT/PD image sensor flat panel of active area: 35.04cm×42.54cm. The sensor plate of Mars1417XF-CSI Wireless Digital Flat Panel Detector is directdeposited with CsI scintillator to achieve the conversion from X-ray to visible photon. The visible photons are transformed to electron signals by diode capacitor array within TFT panel, which are composed and processed by connecting to scanning and readout electronics, consequently to form a panel image by transmitting to PC through the user interface. The major function of the Mars1417XF-CSI Wireless Digital Flat Panel Detector is to convert the X-ray to digital image, with the application of high resolution X-ray imaging. This detector is the key component of DR system, enables to complete the digitalization of the medical X-ray imaging with the DR system software. #### 6. Intended Use [21 CFR 807.92(a)(5)] #### 6.1. Intended Use Mars1417XF-CSI Wireless Digital Flat Panel Detector is indicated for digital imaging solution designed for providing general radiographic diagnosis of human anatomy. It is intended to replace radiographic film/screen systems in all generalpurpose diagnostic procedures. This device is not intended for mammography or dental applications. # 3 of 9 ### [510(k)] Application {5}------------------------------------------------ [510(k)] Application ## iRay Technology Taicang Ltd. # 6.2. Suitable patient It is suitable for providing digital X-ray imaging for DR system conventional photography but not intended for mammography or dental applications. The remaining notes depend on the DR system. ## 6.3. Processing of input and output When flat panel detector works continuously, it can automatically distinguish Xray and output an imaging for diagnosis of disease, injury, or of any applicable health problem. | Item | Predicate Device: Wireless Digital Flat Panel Detector | Proposed Device: Wireless Digital Flat Panel Detector | | | |---------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | 510(K) Number | K161730 | To be assigned | | | | Intended Use | The Mars1417V-PSI Wireless Digital Flat Panel Detector is indicated for digital imaging solution designed for providing general radiographic system in all general purpose diagnostic procedures. | Same | | | | Classification Name | Stationary X-ray system | Same | | | | Product Code | MQB | Same | | | | Item | Predicate Device: Wireless Digital Flat Panel Detector | Proposed Device: Wireless Digital Flat Panel Detector | | | | Regulation Number | 21 CFR 892.1680 | Same | | | | Panel: | Radiology | Same | | | | Classification: | II | Same | | | | X-Ray Absorber (Scintillator): | Gd2O2S | CsI | | | | Installation Type: | Wireless, Portable | Same | | | | Readout Mechanism: | Thin Film Transistor | Same | | | | Image Matrix Size: | 2304 × 2800 pixels | 2336× 2836 pixels | | | | Pixel Pitch: | 150μm | Same | | | | ADC Digitization | 14 bit | 16 bit | | | | Effective Imaging Area: | 355 mm × 434 mm | 350.4 mm × 425.4 mm | | | | Spatial Resolution: | Min. 3.4lp/mm | Min. 3.3lp/mm | | | | Modulation Transfer Function (MTF) | 0.48 at 1 lp/mm | 0.5 at 1 lp/mm | | | | Detective Quantum Efficiency (DQE) | 0.20 at 1 lp/mm (RQA5, 3.2µGy) | 0.37 at 1 lp/mm (RQA5, 2.5µGy) | | | | Power Consumption: | Max. 13W | Max. 19W | | | | Item | Predicate Device: Wireless Digital Flat Panel Detector | Proposed Device: Wireless Digital Flat Panel Detector | | | | Communications: | Wired: Gigabit Ethernet (1000BASE-T) Wireless: IEEE 802.11a/b/g/n (2.4 GHz / 5 GHz) | Wireless: IEEE 802.11a/b/g/n (2.4 GHz / 5 GHz) | | | | | Imaging protect Plate: | Carbon Fiber Plate | Same | | | Cooling: | Air cooling | Same | | | | Dimensions: | $384 \text{ mm } \times 460 \text{ mm } \times 15 \text{ mm}$ | Same | | | | Operation: | Temperature: +5 ~ +35°C Humidity: 30 ~ 75% (Non-Condensing) Atmospheric pressure: 70 ~ 106 kPa Altitude: Max. 3000 meters | Temperature: +5 ~ +30°C Humidity: 10 ~ 80% (Non-Condensing) Atmospheric pressure: 70 ~ 106 kPa Altitude: Max. 3000 meters | | | | | Storage and Transportation: (detector) | Temperature: -20 ~ +55°C Humidity: 10 ~ 90% (Non-Condensing) Atmospheric pressure: 70 ~ 106 kPa Altitude: Max. 3000 meters | Temperature: -20 ~ +50°C Humidity: 10 ~ 90% (Non-Condensing) Atmospheric pressure: 70 ~ 106 kPa Altitude: Max. 3000 meters | | | | | Item | Predicate Device: | Proposed Device: | | | | | Wireless Digital Flat | Wireless Digital Flat | | | | | Panel Detector | Panel Detector | | | | Software | iRay DR The iRay DR used for getting Digital X -ray radiography images from the flat panel detectors. iRay DR is used to handle the DICOM protocol (DICOM 3.0), iRay DR is responsible for the DR equipment management, acquisition and processing functions, to provide patient registration, scanning, image processing, image forwarding, image printing and other functions. | iRay SDK(include iDetector) is intend to supply API interface for DR system manufacturers. DR system manufacturer control the detector by SDK interface. SDK is not intend to use directly by other users beside DR system manufacturers. | ## 7. Technological Characteristic [21 CFR 807.92(a)(6)] {6}------------------------------------------------ # iRay Technology Taicang Ltd. # [510(k)] Application {7}------------------------------------------------ # iRay Technology Taicang Ltd. # [510(k)] Application {8}------------------------------------------------ # iRay Technology Taicang Ltd. ## [510(k)] Application ## 8. System requirements to operate with other radiographic system components - 1) Recommended Generator Specification: Energy range: 40~150kVp mA range: 10~1000mA (depending on the generator power) ms range: 10~6300ms to produce 0.1~1000mAs (depending on the generator power) Note: To our best knowledge, the detector is compatible with the X-ray generators with the specifications described above. If you have any questions regarding the # 7 of 9 {9}------------------------------------------------ ## [510(k)] Application compatibility issue for other generators, please contact your distributor or iRay's service office. - 2) Application Program Interface (API) for system integration manufacturer Peripheral hardware: Mars1417XF-CSI detector connected via wireless communication. | Operating System: | Windows XP/7 32/64bit | |-------------------|------------------------------------------------------------------------| | CPU: | Intel Core i5 3.6G | | Memory: | 8G DDR3 | | Hard Disk: | 640 G | | LAN Card: | Intel Pro EXP9301CT PRO Gigabit Network Adapter with PCIe interface | - 3) X-ray exposure mode The AED trigger module is a unit can connect X-ray signal in the Mars1417XF-CSI. Once there is X-ray generator exposure exist, the inner trigger module will detect the X-ray radiation and output signal to the detector. Until the exposure finished, the detector will receive a signal which represent the end of exposure from the inner trigger module and begin to acquire the image. ### 9. Substantial Equivalence [21 CFR 807.92(b)(1) and 807.92(b)(2)| - 1) Electrical Safety and EMC testing: Electrical, mechanical, environmental safety and performance testing according to IEC/ES 60601-1 was performed, and EMC testing was also conducted in accordance with IEC 60601-1-2. All test results are meet the standard requirements. - 2) Biological Evaluation: The materials of the detector which contact operators' or patient's skin have been evaluated with the ISO 10993-1. And the evaluation results and test result assured the safety the same as the predicate device. - 3) Nonclinical Considerations: {10}------------------------------------------------ ## [510(k)] Application The non-clinical studies have been performed and the results have shown that the Mars1417XF-CSI wireless digital X-ray flat panel detector is substantially equivalent to the predicate devices on the Market (Mars1417V-PSI, K161730 ): Detective quantum efficiency (DQE), Quantum limited performance, Modulation transfer function (MTF), Effects of aliasing, Sensitivity linearity, Lag, Change in detection sensitivity, Dose requirement and reciprocity changes, Stability of device characteristics with time, Uniformity of device characteristic, Noise power spectrum(NPS), Spatial resolution, Image Acquisition time, and Black level. According to the Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices, the software SDK classifies the hazards, defines requirements specification and design specification, all the specification pass the 16 test cases and complies the intended design specification. #### 4) Clinical Consideration: A concurrence study of 30 images was conducted to compare the performance of the Mars1417XF-CSI to that of the predicate device (Mars1417V-PSI, K161730 ). Phantom images were provided; these images were not necessary to establish substantial equivalence based on the differences from the predicate but they provide further evidence in addition to the laboratory performance data to show that the complete system works as intended. There was no significant difference between the images of the Mars1417XF-CSI and those of the predicate device. ### 10. Conclusion [21 CFR 807.92(b)(3)] In accordance with the Federal Food, Drug and Cosmetic Act, 21 CFR Part 807 and based on the information provided in this premarket notification, iRay Technology Taicang Ltd. Concludes that iRay Mars1417XF-CSI Wireless Digital Flat Panel Detectors is substantially equivalent to predicate device with regards to safety and effectiveness.