(141 days)
Not Found
No
The summary describes a standard portable digital X-ray system and does not mention any AI or ML capabilities in the device description, intended use, or performance studies. The "Mentions AI, DNN, or ML" field is explicitly marked as "Not Found".
No.
Explanation: The device is an X-ray imaging system intended for acquiring diagnostic images, not for therapeutic purposes.
No
Explanation: The device is an X-ray imaging system intended for acquiring images of patient anatomy. While these images may be used for diagnostic purposes by a physician, the device itself acquires the images; it does not directly perform a diagnosis or provide diagnostic interpretations.
No
The device description explicitly lists hardware components: a portable X-ray unit, a flat panel detector, and a workstation. This indicates it is a hardware system with integrated software, not a software-only device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states the purpose is "acquiring X-ray images of the desired parts of patient's anatomy". This is a diagnostic imaging device, not a device used to examine specimens derived from the human body (like blood, urine, or tissue) to provide information for diagnosis, monitoring, or treatment.
- Device Description: The description details components like a portable X-ray unit, flat panel detector, and workstation, all consistent with an X-ray imaging system.
- Input Imaging Modality: The input modality is X-ray, which is an imaging technique applied directly to the patient, not a method for analyzing in vitro samples.
IVD devices are specifically designed to perform tests on samples taken from the body, outside of the body (in vitro). This device operates by generating X-rays that pass through the patient's body to create an image.
N/A
Intended Use / Indications for Use
Intended for use by a qualified/trained physician or technician for the purpose of acquiring X-ray images of the desired parts of patient's anatomy (including head, cervical spine, chest, abdomen, lumbar spine, pelvis and extremities).This device is not intended for mammography.
Product codes (comma separated list FDA assigned to the subject device)
IZL, MQB, LLZ
Device Description
This SR-1000/SR-1000S Portable DR Imaging System is a portable digital device developed, designed and manufactured by SIUI. A detailed comparison table with an equivalent device is provided below. The device consists of the following major components: a portable X-ray unit, a flat panel detector, and workstation. The difference between SR-1000 and SR-1000S is the operation interface of the portable X-ray Unit only, while the flat panel detector and the workstation are the same for SR-1000 and SR-1000S. The SR-1000S has the display interface with button-operation digital tube, while the SR-1000 has the display interface with touch screen operation. Except for the difference above, the 2 models (SR-1000 and SR-1000S) are completely the same in all the other mechanical and circuit design. The major components of the X-ray main unit include: handle, enclosure, control panel, system control (SYS) board, high-voltage tank, collimator (beam limiter), lithium-ion battery and system control software running on the SYS board.
The system control software is for real-time interaction and control with various circuit modules inside the Portable DR Imaging System. The software responds to user operations on the control panel. The user can adjust and control the kV and mAs parameters, and the software will display the parameters or directly load the APR parameters. The software loads the control data from X-ray output into the high-voltage generation control circuit of the system control board, and control the high-voltage tank to generate high-voltage to excite the X-ray tube inside to emit X-rays, control the switch of the collimator indicator, and monitor the working status of the device, the battery power status, and control the display of the status indicators. The system is for X-ray imaging and diagnosis in facilities with mobile or fixing sites. Since the kV range of this device is 40~125kVp, which is not suitable for breast exams, the device is not intended for mammography.
The flat panel detector is the core of image acquisition of the system. The X-ray emitted through the human body is converted by the scintillator of flat panel detector to visible optical signals, which are then converted to digital signals by the amorphous silicon of flat panel detector. The processed digital signals are sent to the image workstation for image reconstruction, display, storage and transmission via a Gigabit Ethernet cable. The image workstation is installed with a PIE-5 DR Workstation, which is the core of image acquisition and processing on the system.
Mentions image processing
Yes
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
X-ray
Anatomical Site
head, cervical spine, chest, abdomen, lumbar spine, pelvis and extremities
Indicated Patient Age Range
Not Found
Intended User / Care Setting
qualified/trained physician or technician
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Clinical testing is not necessary for the SR-1000/SR-1000S Portable DR Imaging System in order to demonstrate substantial equivalence to the predicate device.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
AcuityPDR (K200726)
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 892.1720 Mobile x-ray system.
(a)
Identification. A mobile x-ray system is a transportable device system intended to be used to generate and control x-ray for diagnostic procedures. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.(b)
Classification. Class II.
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.
Shantou Institute of Ultrasonic Instruments Co., Ltd. (SIUI) % Flower Cai Liaison Manager 77 Jinsha Road Shantou, Guangdong 515041 CHINA
Re: K202350
Trade/Device Name: SR-1000 Portable DR Imaging System, SR-1000S Portable DR Imaging System Regulation Number: 21 CFR 892.1720 Regulation Name: Mobile X-Ray System Regulatory Class: Class II Product Code: IZL, MQB, LLZ Dated: November 20, 2020 Received: November 23, 2020
January 6, 2021
Dear Flower Cai:
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. Although this letter refers to your product as a device, please be aware 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.
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 requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part
1
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/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) 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 https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). 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 (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
For
Thalia T. Mills, Ph.D. Director Division of Radiological Health OHT7: Office of In Vitro Diagnostics and Radiological Health Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known) K202350
Device Name
SR-1000 Portable DR Imaging System SR-1000S Portable DR Imaging System
Indications for Use (Describe)
Intended for use by a qualified/trained physician or the purpose of acquiring X-ray images of the desired parts of patient's anatomy (including head, cervical spine, chest, abdomen, lumbar spine, pelvis and extremities).This device is not intended for mammography.
Type of Use (Select one or both, as applicable)
| ☑ Prescription Use (Part 21 CFR 801 Subpart D) | ☐ Over-The-Counter Use (21 CFR 801 Subpart C) |
|---|---|
| ---------------------------------------------------------------------------------------------------------- | --------------------------------------------------------------------------------------------------------- |
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3
510(k) Summary
This summary of 510(k) safety and effectiveness information is provided in accordance with the requirements of SMDA 1990 and 21 CFR 807.92(c).
The assigned 510(k) number is: K202350
5.1 Submitter
Shantou Institute of Ultrasonic Instruments Co., Ltd. (SIUI)
77 Jinsha Road, Shantou, Guangdong 515041, China
Tel: 86-754-88250150
Fax: 86-754-88251499
Contact Person: Flower Cai
Shantou Institute of Ultrasonic Instruments Co., Ltd.
77 Jinsha Road, Shantou, Guangdong 515041, China
Date Prepared: Aug 19, 2020
5.2 Device
Name of Device: SR-1000 Portable DR Imaging System
SR-1000S Portable DR Imaging System
Classification Name: Mobile x-ray system (21 CFR 892.1720)
Regulatory Class: II
Product Code: IZL, MQB, LLZ
Predicate Device 5.3
The SR-1000/SR-1000S Portable DR Imaging System is for X-ray imaging and diagnosis, image acquisition in facilities with mobile or fixing sites, and is substantially equivalent to the predicate device.
Name of Predicate Device: AcuityPDR (K200726)
4
Classification Name: Mobile x-ray system (21 CFR 892.1720)
Regulatory Class: II
Product Code: IZL, MQB, LLZ
5.4 Device Description
This SR-1000/SR-1000S Portable DR Imaging System is a portable digital device developed, designed and manufactured by SIUI. A detailed comparison table with an equivalent device is provided below. The device consists of the following major components: a portable X-ray unit, a flat panel detector, and workstation. The difference between SR-1000 and SR-1000S is the operation interface of the portable X-ray Unit only, while the flat panel detector and the workstation are the same for SR-1000 and SR-1000S. The SR-1000S has the display interface with button-operation digital tube, while the SR-1000 has the display interface with touch screen operation. Except for the difference above, the 2 models (SR-1000 and SR-1000S) are completely the same in all the other mechanical and circuit design. See the photos below (Fig. 1 and Fig. 2).
Image /page/4/Picture/6 description: The image shows a portable X-ray machine. The machine consists of a detector, an X-ray source, and a laptop. The detector is a flat panel that captures the X-ray image. The X-ray source emits X-rays that pass through the object being imaged. The laptop is used to control the X-ray source and to display the X-ray image. The machine is housed in a rugged case for easy transport.
Fig.1 SR-1000S Portable DR Imaging System
5
Image /page/5/Picture/1 description: The image shows a portable X-ray machine. The machine consists of a detector panel, an X-ray source, and a laptop. The detector panel is a flat, rectangular device that is used to capture the X-ray image. The X-ray source is a small, handheld device that emits X-rays. The laptop is used to control the X-ray source and to view the X-ray image.
Fig.2 SR-1000 Portable DR Imaging System
The major components of the X-ray main unit include: handle, enclosure, control panel, system control (SYS) board, high-voltage tank, collimator (beam limiter), lithium-ion battery and system control software running on the SYS board.
The system control software is for real-time interaction and control with various circuit modules inside the Portable DR Imaging System. The software responds to user operations on the control panel. The user can adjust and control the kV and mAs parameters, and the software will display the parameters or directly load the APR parameters. The software loads the control data from X-ray output into the high-voltage generation control circuit of the system control board, and control the high-voltage tank to generate high-voltage to excite the X-ray tube inside to emit X-rays, control the switch of the collimator indicator, and monitor the working status of the device, the battery power status, and control the display of the status indicators. The system is for X-ray imaging and diagnosis in facilities with mobile or fixing sites. Since the kV range of this device is 40~125kVp, which is not suitable for breast
The flat panel detector is the core of image acquisition of the system. The X-ray emitted through the human body is converted by the scintillator of flat panel detector to visible optical signals, which are then converted to digital signals by the amorphous TAB 2 Section 5 510(k) Summary Page 3 of 9
exams, the device is not intended for mammography.
6
silicon of flat panel detector. The processed digital signals are sent to the image workstation for image reconstruction, display, storage and transmission via a Gigabit Ethernet cable. The image workstation is installed with a PIE-5 DR Workstation, which is the core of image acquisition and processing on the system.
5.5 Indications for Use
Intended for use by a qualified/trained physician or technician for the purpose of acquiring X-ray images of the desired parts of patient's anatomy (including head, cervical spine, chest, abdomen, lumbar spine, pelvis and extremities).This device is not intended for mammography.
Comparison of Technological Characteristics with the Predicate Device 5.6
The comparison between the overall specifications of the predicate device (AcuityPDR) and the new device (SR-1000/SR-1000S) is shown in Table 1. Any differences between the predicate and the new device have no impact on safety or efficacy of the new device and do not raise any new potential or increased safety risks, and the new device is equivalent in performance to existing legally marketed devices.
| Description | Predicate Device
AcuityPDR (K200726) | Subject Device
SR-1000/SR-1000S | |
|---------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------|
| Indications for use | Intended for use by a
qualified/trained physician
or technician on both adult
and pediatric subjects for
taking diagnostic x-rays.
Not for mammography. | Intended for use by a
qualified/trained physician or
technician for the purpose of
acquiring X-ray images of the
desired parts of patient's anatomy
(including head, cervical spine,
chest, abdomen, lumbar spine,
pelvis and extremities).This device
is not intended for mammography. | |
| X-ray Generator(s) Model | -- | SR-8100 (K200637) or
SR-8100S | |
| Generator Photos | Image: AcuityPDR Generator | SR-8100
Image: SR-8100 Generator
SR-8100S
Image: SR-8100S Generator | |
| Description | | Predicate Device
AcuityPDR (K200726) | Subject Device
SR-1000/SR-1000S |
| Basic
Generator
Characteristics | Peak
generator | 2kW | 2kW |
| | Tube
current | 40-60kV:25mA
61-100kV:20mA | 40-60kV:25mA
61-100kV:20mA |
| | Tube
voltage
adjustable
range | 40-100kV, step value 1kV | 40-100kV, step value 1kV |
| | mAs range | 0.4mAs-50mAs,with the
range of :
0.40,0.50,0.63,0.80,1.00,1.2
5,1.6,2.0,2.5,3.2,4.0,5.0,6.3,
8,10,12.5,16,20,25,32,40,50 | 0.4mAs-50mAs,with the range of :
0.40,0.50,0.63,0.80,1.00,1.25,1.6,2
.0,2.5,3.2,4.0,5.0,6.3,8,10,12.5,16,
20,25,32,40,50 |
| Collimator | | Built in | Built in |
| X-ray Generator | | One model, up to 100kVp | One model, up to 100kVp |
| Operator console | | Touch Control or Touch
Screen | Button Control or Touch Screen |
| Digital X-Ray Detectors | | AcuityDR (K171137) | SFD-1X |
| Panel Shape | | Rectangular Panel | Rectangular Panel |
| Detector Size | | 13" X 17" | 14" X 17" |
| Pixel Pitch | | 140 μ m | 150 μm |
| Materials Scintillator | | TFT-amorphous
Silicon | TFT-amorphous
Silicon |
| DQE | | 25% at 1.0 lp/mm
5% at 3.0 lp/mm | 46.7% at 1.0 lp/mm
21.7% at 3.0 lp/mm |
| MTF | | 35% at 2.0 lp/mm | 47.3% at 2.0 lp/mm |
| Communication
Method | | Wire
Wireless
IEEE 802.11a//g/n(2.4GHz/
5GHz)
Security: WEP/WPA/WPA2 | Wire
Wireless
IEEE 802.11a//g/n(2.4GHz/
5GHz)
Security: WEP/WPA/WPA2 |
| Acquisition Software | | AccuVueMED (K152172) | PIE-5 |
| Software function | | Image viewing
Image search
Image storage | Image viewing
Image search
Image storage |
| Description | Predicate Device
AcuityPDR (K200726) | Subject Device
SR-1000/SR-1000S | |
| | Image annotation
Image measurement
Image processing
Image stitch | Image annotation
Image measurement
Image processing
Image stitch | |
| DICOM 3.0 Compatibility | Yes | Yes | |
| Photos | Image: AcuityPDR (K200726) | Image: SR-1000/SR-1000S
Note: The portable stand is an
optional component. | |
| Power Source | AC Line or rechargeable
batteries (Generator only) | AC Line or rechargeable batteries | |
7
SIUI SR-1000/SR-1000S Portable DR Imaging System
8
5.7 Non-clinical Testing Summary
The SR-1000/SR-1000S Portable DR Imaging System complies with and/or was tested in accordance with the following FDA guidance and International Standards:
- IEC 60601-1: 2005+A1:2012 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
- . IEC60601-1-2: 2014 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests.
- . IEC60601-2-54:2009+A1:2015+A2:2018 Medical electrical equipment - Part 2-54:Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy
- . IEC60601-1-3: 2008+A1:2013 Medical electrical equipment Part 1-3: General requirements for basic safety and essential performance - Collateral standard:
9
Radiation protection in diagnostic X-ray equipment
- ISO 14971: 2007 Medical device - Application of risk management to medical devices
- ISO 10993-1: 2018 Biological evaluation of medical devices-Part1: Evaluation and testing within a risk management process
- ISO 10993-5:2009 Biological evaluation of medical devices-Part5: Tests for in vitro cytotoxicity
- . ISO 10993-10:2010 Biological evaluation of medical devices - Part 10:Tests for irritation and skin sensitization
- IEC 62304:2006+AMD1:2015 Medical device software = Software life cycle processes
- IEC 60601-1-6:2010+A1:2013 Medical electrical equipment Part 1-6: General requirements for basic safety and essential performance - collateral standard: Usability
- IEC 62366-1:2015/COR1:2016 Medical devices - Application of usability engineering to medical devices
- . ISO 15223-1:2016 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements
- ISO 13485 :2016 Medical devices - Quality management systems - Requirements for regulatory purposes
- Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices
- . Content of Premarket Submissions for Management of Cybersecurity in Medical Devices
- Radio Frequency Wireless Technology in Medical Devices
- Guidance for the Pediatric Information for X-ray Imaging Device Premarket Notifications
The subject device and the predicate device are comparable in terms of technical features, general functions, applications and intended uses. The test results showed compliance with the above standards. Validation was performed for overall operation by taking and reviewing test images. The non-clinical tests demonstrate that the device is as safe, as effective, and performs as well as the predicate.
10
Software Description 5.8
The SR-1000/SR-1000S Portable DR Imaging System contains two software, one is the embedded software in the X-ray unit: system control software, and the other is PIE-5 DR Workstation (herein after referred to as "PIE-5").
The system control software of SR-1000/SR-1000S is new software designed by SIUI. The software adopts development languages of keil, the program language is C language, the hardware platform is ARM. The system control software is for real-time interaction and control with various circuit modules inside the Portable DR Imaging System. The software responds to user operations on the control panel. The user can adjust and control the kV and mAs parameters, and the software will display the parameters or directly load the APR parameters. The software loads the control data from X-ray output into the high-voltage generation control circuit of the system control board, control the high-voltage tank to generate high-voltage to excite the X-ray tube inside to emit X-rays, control the switch of the collimator indicator, monitor the working status of the device and the battery power status, and control the display of the status indicators. The Level of Concern for the Software Device is Moderate.
The programming language of PIE-5 is C language, and the operating platform is Microsoft Windows. The software is a medical image processing system, consisting of image acquisition, image review and diagnosis, image processing and digital storage functions, which mainly address digital image workflow in radiographic department of hospitals. The functions of the software include patient registration. image acquisition and processing, image review and diagnosis, image printing, report editing and PACS transmission, digital image storage and recovery. The Level of Concern for the Software Device is Moderate.
5.9 Clinical Testing
Clinical testing is not necessary for the SR-1000/SR-1000S Portable DR Imaging System in order to demonstrate substantial equivalence to the predicate device.
5.10 Conclusion
The subject device SR-1000/SR-1000S system and the predicate device are comparable in terms of technical features, general functions, applications and indications for use.
11
Compared with the predicate device, the power of the SR-1000/SR-1000S is higher. The SR-1000/SR-1000S can be used for imaging including head, cervical spine, chest, abdomen, lumbar spine, pelvis and extremities, and the predicate device AcuityPDR can be used for both adult and pediatric subjects for taking diagnostic x-rays. Nevertheless, it does not affect the safety and effectiveness of the SR-1000/SR-1000S, nor does it change the indications for use of the SR-1000/SR-1000S unit.
The indications for use of the SR-1000/SR-1000S Portable DR Imaging System do not create new potential safety risks, and its performance is comparable as that of the marketed products. Therefore, the device is as safe and effective as the legally marketed predicate device.