(55 days)
The Heart5R-110. Heart3R-110 are Portable X-ray Machine, intended for use by a qualified/trained physician or technician on adult population 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).
The system is subject to the following limitations of use when stand-mounted:
- The device may be used for diagnostic imaging of head, cervical spine, abdomen, lumbar spine, pelvis or extremities. -The device may be used for imaging of the chest when used without a grid.
This device is not intended for mammography.
The Portable X-ray machine directly provides rays for diagnostic operation, which is composed of the following parts: power supply circuit, inverter, high-voltage tank ball tube, filament circuit, control circuit, high-voltage cabinet body, user interface and collimator.
This document is a 510(k) summary for a portable X-ray machine. It demonstrates substantial equivalence to a predicate device rather than providing acceptance criteria and a study proving the device meets those criteria. Therefore, most of the requested information cannot be extracted directly from the provided text.
However, I can provide the following based on the available information:
1. Table of Acceptance Criteria and Reported Device Performance:
The document does not explicitly state "acceptance criteria" in terms of specific performance metrics for the device to meet. Instead, it compares the specifications of the subject device to a predicate device to establish substantial equivalence.
Comparison of Subject Device (Heart5R-110, Heart3R-110) vs. Predicate Device (SR-8230/SR-8230S):
| Description | Subject Device (Heart5R-110, Heart3R-110) Performance | Predicate Device (SR-8230/SR-8230S) Performance |
|---|---|---|
| Indications for Use | Acquiring X-ray images of adult anatomy (head, cervical spine, chest, abdomen, lumbar spine, pelvis, extremities). Head, cervical spine, abdomen, lumbar spine, pelvis or extremities when stand-mounted. Chest imaging without a grid when stand-mounted. Not for mammography. | Acquiring X-ray images of adult anatomy (head, cervical spine, chest, abdomen, lumbar spine, pelvis, extremities). Handheld diagnostic imaging of body extremities. Head, cervical spine, abdomen, lumbar spine, pelvis or extremities when stand-mounted. Chest imaging without a grid when stand-mounted. Not for mammography. |
| Weight | 17.6kg (Including Collimator) | 15kgs (33.06lb) (Including Collimator) |
| Size | 367mm×251mm×228mm | 460mm×245mm×188mm |
| Use Interface | Soft touch push buttons | SR-8230: Soft touch push buttons; SR-8230S: Touch screen |
| Exposure time | 0.001sec~2sec : R'20 sec Step | 0.02 sec - 6.3 sec: R'10 sec Step |
| Memory Settings (technique) | 14 memories | 16 memories |
| HF Generator | High Frequency | High Frequency |
| kW | 5.0KW (Heart5R-110), 3.0KW (Heart3R-110) | 5.0kW |
| kVp | 40-125kVp | 40-125kVp |
| mA | 10mA-100mA (Heart5R-110), 10mA-71mA (Heart3R-110): R'20 sec Step | 10mA-100mA: R'10 sec Step |
| FDA Performance Standard | Complies | Complies |
| Collimator Model | CRUX707i | SIUI SR-8200-39L |
| Collimator Manufacturer | Yian | SIUI |
| Collimator Control | Manual control | Manual with 15, 30, 45, 60sec. Lamp timer |
| Output Rating | Max. 5.0kW (50mA@100kV) | Max. 5.0kW (40mA@125kV) |
| Type | Microprocessor controlled High Frequency inverter | Microprocessor controlled High Frequency inverter |
| kV Range | 40~125kV, 86 Step (1kV Step) | 40~125kV, 86 Step (1kV Step) |
| mA Range | 10~100mA, 21 Steps (10,11,12.5,14,16,18,20,22,25,28,32,36,40,45,50,56,63,71,80,90,100mA) | 10~100mA, 11 Steps (10,12.5,16,20,25,32,40,50,64,80,100mA) |
| Exposure Time | 0.001sec~2sec : R'20 sec Step | 0.02~6.3 seconds, 26 Step (in 25% Steps) |
| mAs Range | 0.1~100mAs, 50 Step | 0.4~200mAs, 28 Step (in 25% Steps) |
| X-ray Tube Type | Stationary Anode | Stationary Anode |
| Focal Spot Size (Small/Large) | 0.6/1.8mm | 0.6/1.8mm |
| Anode Heat Storage Capacity | 42,000HU | 42,000HU (30,000J) |
| Power Cord Length | 2.08m | 3m |
| Exposure Hand-switch Cord Length | 5m | 6m (Max. Length) |
| X-ray switching frequency | 60KHZ | 100kHz |
| Control | 2 Point Control (kV, mAs) | 2 Point Control (kV, mAs) |
| Anatomical Programs | Preprogrammed 16 APR data - User Programmable | Preprogrammed 16 APR data - User Programmable |
| Field Shape (Collimator) | Rectangular | Rectangular |
| Max. Field Size (Collimator) | 43x43cm (at 100cm SID) | 44x44cm (at 100cm SID) |
| Leakage Radiation (Collimator) | < 1mGyh. (at SID 1m) | < 40mR/hr. (at SID 1m) |
| Max. kVp shield (Collimator) | 150kV | 150kV |
| Inherent Filtration (Collimator) | 1.0mmAl eq. | 1.2mmAl eq. |
| Light source (Collimator) | 9W LED | 9W LED |
| Standard (Collimator) | Rotating flange | Rotating flange |
| Option (Collimator) | Ultrasonic distance measurement (Max.180cm) | Tape measure (Max.200cm) |
| Electrical Rating (Collimator) | 24V AC/DC, Max.4A | 3-12VDC, 10W |
| Dimension/weight (Collimator) | 139.3(W) × 166.5(D) × 83(H)mm / 1.5kg | 170(W)×180(D)×105(H) mm / 1.2kg(2.65lb) |
2. Sample Size Used for the Test Set and Data Provenance:
The document explicitly states: "The subject of this premarket submission, did not require clinical studies to support substantial equivalence." This means there was no specific test set of patient data used for clinical evaluation. The evaluation was based on non-clinical (bench) testing and comparison to an existing predicate device.
3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications of Those Experts:
Not applicable, as no clinical studies with a test set requiring expert ground truth were conducted.
4. Adjudication Method for the Test Set:
Not applicable, as no clinical studies with a test set requiring adjudication were conducted.
5. If a Multi Reader Multi Case (MRMC) Comparative Effectiveness Study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance:
Not applicable. This device is a portable X-ray machine, not an AI or image analysis software. The summary explicitly states: "The software is Moderate level of concern, it is original software, and it is not a software for image analysis."
6. If a Standalone (i.e. algorithm only without human-in-the-loop performance) was done:
Not applicable, as this is a hardware device (X-ray machine) and its software is not for image analysis.
7. The Type of Ground Truth Used:
Not applicable for clinical ground truth. The "ground truth" for this submission focuses on compliance with established engineering and safety standards, and ensuring physical and functional equivalence to the predicate device through non-clinical testing.
8. The Sample Size for the Training Set:
Not applicable, as this device does not involve AI or machine learning models that require a training set.
9. How the Ground Truth for the Training Set was Established:
Not applicable.
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May 4, 2022
Yian Medical Technology (Haining) Co., Ltd Zhiqin Yu RA Supervisor 1st Floor Area 1, 2nd Floor Area 1, Building A, No. 2 Caohejing Road, Haining Economic Development Zone Jiaxing, Zhejiang CHINA
Re: K220700
Trade/Device Name: Heart5R-110 Portable X-Ray Machine, Heart3R-110 Portable X-ray Machine Regulation Number: 21 CFR 892.1720 Regulation Name: Mobile x-ray system Regulatory Class: Class II Product Code: IZL Dated: February 28, 2022 Received: March 10, 2022
Dear Zhigin Yu:
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
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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 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,
Laurel Burk, Ph.D. Assistant Director Diagnostic X-ray Systems Team DHT 8B: Division of Radiological Imaging and Electronic Products OHT8: Office of Radiological Health Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
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Section 4: Indications for Use Statement (FDA form 3881)
Heart5R-110, Heart3R-110 Portable X-ray Machine
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Indications for Use
510(k) Number (if known) K220700
Device Name Heart5R-110 Portable X-ray Machine Heart3R-110 Portable X-ray Machine
Indications for Use (Describe)
The Heart5R-110. Heart3R-110 are Portable X-ray Machine, intended for use by a qualified/trained physician or technician on adult population 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).
The system is subject to the following limitations of use when stand-mounted:
- The device may be used for diagnostic imaging of head, cervical spine, abdomen, lumbar spine, pelvis or extremities. -The device may be used for imaging of the chest when used without a grid.
This device is not intended for mammography.
Type of Use (Select one or both, as applicable)
X Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
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Section 5: 510(k) Summary
Heart5R-110, Heart3R-110 Portable X-ray Machine
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510(k) Summary (K220700)
| Date Prepared: | Feb 28, 2022 |
|---|---|
| Manufacturer: | Yian Medical Technology (Haining) Co., Ltd1st Floor Area 1, 2nd Floor Area 1, Building A,No. 2 Caohejing Road, Haining EconomicDevelopment Zone, Haichang Street, HainingCity, Jiaxing City, Zhejiang Province, China |
Contact Person: Zhiqin Yu RA Supervisor Yian Medical Technology (Haining) Co., Ltd Tel: +86-0573-87217250 zhiqin.yu@yian-medical.com
ldentification of the Device:
| Proprietary/Trade Name: | Heart 5R-110 Portable X-Ray MachineHeart 3R-110 Portable X-Ray Machine |
|---|---|
| Classification Name: | Mobile x-ray system |
| Regulatory Number: | 21 CFR Part 892.1720 |
| Product Code: | IZL |
| Device Class: | Class II |
| Review Panel: | Radiology |
Identification of the Legally Marketed Predicate Device:
| Trade Name: | SR-8230 Portable X-ray Unit |
|---|---|
| SR-8230S Portable X-ray Unit | |
| Classification Name: | Mobile x-ray system |
| Regulatory Number: | 21 CFR Part 892.1720 |
| Product Code: | IZL |
| Device Class: | Class II |
| Review Panel: | Radiology |
| Submitter/510(k) Holder: | Shantou Institute of Ultrasonic Instruments Co.Ltd. (SIUI). |
| Clearance: | K200976 (cleared June 10, 2020) |
Device Description:
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The Portable X-ray machine directly provides rays for diagnostic operation, which is composed of the following parts: power supply circuit, inverter, high-voltage tank ball tube, filament circuit, control circuit, high-voltage cabinet body, user interface and collimator.
| Model | Heart 5R-110 | Heart 3R-110 |
|---|---|---|
| Power | 5KW | 3KW |
| KV range | 40 to 125 kV | |
| KV precision | $\leq \pm 8%$ | |
| mA range | 10mA to 100mA | 10mA to 71mA |
| mA precision | $\leq \pm 20%$ | |
| ms range | 1~2000ms | |
| ms precision | $\leq \pm (10%+1ms)$ | |
| mAs range | 0.1mAs to 100mAs | |
| mAs precision | $\leq \pm (10%+0.2mAs)$ | |
| Nominal focus size | 0.6/1.8 | |
| The anode target Angle | 15° | |
| Tube core inherentlyfiltered | 0.65mmAL/75KV |
The differences between the Heart 5R and Heart 3R models:
The software is Moderate level of concern, it is original software, and it is not a software for image analysis.
Any x-ray detectors (necessary for a fully-functional x-ray system) are not part of the current submission.
Indications for Use:
The Heart5R-110, Heart3R-110 are Portable X-ray Machine, intended for use by a qualified/trained physician or technician on adult population 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).
The system is subject to the following limitations of use when stand-mounted:
- The device may be used for diagnostic imaging of head, cervical spine, abdomen, lumbar spine, pelvis or extremities.
-The device may be used for imaging of the chest when used without a grid. This device is not intended for mammography.
Standards:
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- ANSI AAMI ES60601-1:2005/(R)2012 and A1:2012, C1:2009/(R)2012 and A A2:2010/(R)2012 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance (IEC 60601-1:2005, MOD)
-
IEC 60601-1-2 Edition 4.0 2014-02Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance -Collateral Standard: Electromagnetic disturbances - Requirements and tests
- IEC 60601-1-3 Edition 2.1 2013-04 Medical electrical equipment Part 1-3: > General requirements for basic safety and essential performance -Collateral Standard: Radiation protection in diagnostic X-ray equipment
-
IEC 60601-1-6 Edition 3.1 2013-10Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance -Collateral standard: Usability
- IEC 60601-2-28 Edition 3.0 2017-06 Medical electrical equipment Part A 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis
- IEC 60601-2-54 Edition 1.2 2018-06 CONSOLIDATED VERSION Medical A electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy
- ISTA 3B 2017 Packaged-Products for Less-Than-Truckload (LTL) A Shipment
-
IEC 62366-1 Edition 1.0 2015-02 Medical devices - Part 1: Application of usability engineering to medical devices [Including CORRIGENDUM 1 (2016)]
- IEC 62304 Edition 1.1 2015-06 CONSOLIDATED VERSION > Medical device software - Software life cycle processes
-
ISO 15223-1 Fourth edition 2021-07 Medical devices - Symbols to be used with medical device labels, labelling, and information to be supplied - Part 1: General requirements
-
ISO 14971 Third Edition 2019-12 Medical devices - Application of risk management to medical devices
-
ISO 20417:2021 - Medical devices-Information to be supplied by the manufacturer
-
FCC Part 15 Radio Frequency Devices of Part 15B and Part 15C
FDA Guidance Documents:
- "Format for Traditional and Abbreviated 510(k)s Guidance" issued on A September 13, 2019.
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- Radio Frequency Wireless Technology in Medical Devices A
- Guidance for Medical X-ray Imaging Devices Conformance with IEC > Standards
Performance standard:
- 21CFR PART 1010 PERFORMANCE STANDARDS FOR ELECTRONIC A PRODUCTS: GENERAL
- A 21 CFR 1020.30: Diagnostic x-ray system and their major components
- A 21 CFR 1020.31: Radiographic Equipment
Comparison with Predicate Device:
The Heart5R-110, Heart3R-110 Portable X-ray Machine and its predicate device, have the equivalent intended use, functions and similar physical characteristics, performance characteristics.
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Substantial Equivalence:
The comparison between the overall specifications of predicate device (SR-8230/SR-8230S) and the new device (Heart5R-110, Heart3R-110) is shown in Table 1, and the comparison between the Collimator specifications of reference device (SR-8230/SR-8230S) and the new device (Heart5R-110, Heart3R-110) is shown in Table 2. 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 | Subject Device | Predicate Device |
|---|---|---|
| Heart5R-110,Heart3R-110 | SR-8230/SR-8230S (K200976) | |
| Indicationsforuse | The Heart5R-110,Heart3R-110 are PortableX-ray Machine, intended foruse by a qualified/trainedphysician or technician onadult population for thepurpose of acquiring X-rayimages of the desired parts ofpatient's anatomy (includinghead, cervical spine, chest,abdomen, lumbar spine, pelvisand extremities).The system is subject to thefollowing limitations of usewhen stand-mounted:- The device may be used fordiagnostic imaging of head,cervical spine, abdomen,lumbar spine, pelvis orextremities.-The device may be used forimaging of the chest whenused without a grid. | The SR-8230/SR-8230SPortable X-ray Unit is aportable X-ray device, intendedfor use by a qualified/trainedphysician or technician for thepurpose of acquiring X-rayimages of the desired parts ofpatient's anatomy (includinghead, cervical spine, chest,abdomen, lumbar spine, pelvisand extremities).The device may be used forhandheld diagnosticimaging of body extremities.The system is subject to thefollowing limitations of usewhen stand-mounted:- The device may be used fordiagnostic imaging of head,cervical spine, abdomen,lumbar spine,pelvis or extremities.-The device may be used forimaging of the chest whenused without a grid. This deviceis not intended |
| Description | Subject Device | Predicate Device |
| Heart5R-110,Heart3R-110 | SR-8230/SR-8230S (K200976) | |
| This device is not intended formammography. | for mammography. | |
| Weight | 17.6kg(Including Collimator) | 15kgs(33.06lb) (IncludingCollimator) |
| Size | 367mm×251mm×228mm | 460mm×245mm×188mm |
| UseInterface | Soft touchpush buttons | SR-8230: Soft touchpush buttonsSR-8230S: Touch screen |
| Exposuretime | 0.001sec~2sec : R'20 sec Step | 0.02 sec - 6.3 sec: R'10 secStep |
| MemorySettings(technique) | 14 memories | 16 memories |
| HFGenerator | High Frequency | High Frequency |
| kW | 5.0KW(Heart5R-110)3.0KW(Heart3R-110) | 5.0kW |
| kVp | 40-125kVp | 40-125kVp |
| mA | 10mA-100mA (Heart5R-110),10mA-71mA (Heart3R-110):R'20 sec Step | 10mA-100mA: R'10 sec Step |
| FDAPerformanceStandard | Complies | Complies |
| Collimator | CRUX707i | SIUI SR-8200-39L |
| OutputRating | Max. 5.0kW(50mA@100kV) | Max. 5.0kW(40mA@125kV) |
| Type | Microprocessor controlledHigh Frequency inverter | Microprocessor controlledHigh Frequency inverter |
| kV Range | 40~125kV,86 Step (1kVStep) | 40~125kV,86 Step (1kVStep) |
| mA Range | 10~100mA,21 Steps(10,11,12.5,14,16,18,20,22,25,28,32,36,40,45,50,56,63,71,80,90,100mA) | 10~100mA, 11 Steps(10,12.5,16,20,25,32,40,50,64,80,100mA) |
| Exposure | 0.001sec~2sec : R'20 sec Step | 0.02~6.3 seconds |
| Description | Subject DeviceHeart5R-110,Heart3R-110 | Predicate DeviceSR-8230/SR-8230S (K200976) |
| Time | 26 Step (in 25% Steps) | |
| mAs | 0.1~100mAs, | 0.4~200mAs, |
| Range | 50 Step | 28 Step ( in 25% Steps) |
| X-ray TubeType | Stationary Anode | Stationary Anode |
| Focal SpotSize(Small/Large) | 0.6/1.8mm | 0.6/1.8mm |
| AnodeHeatStorageCapacity | 42,000HU | 42,000HU (30,000J) |
| PowerCordLength | 2.08m | 3m |
| ExposureHand-switch CordLength | 5m | 6m (Max. Length) |
| X-rayswitchingfrequency | 60KHZ | 100kHz |
| Control | 2 Point Control (kV, mAs) | 2 Point Control (kV, mAs) |
| AnatomicalPrograms | Preprogrammed 16 APR data-User Programmable | Preprogrammed 16 APR data-User Programmable |
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Image /page/11/Picture/0 description: The image contains a logo for IAN MEDICAL. The logo consists of a stylized letter "N" in green and gray, followed by the text "IAN MEDICAL" in gray. Above the text "IAN MEDICAL" are three Chinese characters, also in gray. The logo is simple and modern, and the colors are muted.
Table 2 Collimator Specs Comparison
| Description | Subject Device | Predicate Device |
|---|---|---|
| Heart5R-110,Heart3R-110 | SR-8230/SR-8230S(K200976) | |
| Model | CRUX707i | SR-8200-39L |
| Manufacturer | Yian | SIUI |
| Control | Manual control | Manual with 15, 30, 45,60sec. Lamp timer |
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| Field Shape | Rectangular | Rectangular |
|---|---|---|
| Max. Field Size | 43x43cm (at 100cm SID) | 44x44cm (at 100cm SID) |
| Leakage Radiation | < 1mGyh. (at SID 1m) | < 40mR/hr. (at SID 1m) |
| Max. kVp shield | 150kV | 150kV |
| Inherent Filtration | 1.0mmAl eq. | 1.2mmAl eq. |
| Light source | 9W LED | 9W LED |
| Standard | Rotating flange | Rotating flange |
| Option | Ultrasonic distance measurement (Max.180cm) | Tape measure (Max.200cm) |
| Electrical Rating | 24V AC/DC, Max.4A | 3-12VDC, 10W |
| Dimension/ weight | 139.3(W) × 166.5(D) × 83(H)mm / 1.5kg | 170(W)×180(D)×105(H) mm / 1.2kg(2.65lb) |
The subjected device and the predicted device are identical in the indications for use, patient population, use environment, and electrical safety. They are similar in technical specification. The differences between the proposed device and the predicate device will not raise any new issues of safety or effectiveness.
Summary of Testing:
Summary of Non-Clinical Tests:
Electrical Safety and Electromagnetic Compatibility Summary
The electrical safety and EMC data included in the submission is in compliance with the following FDA recognized standards:
- ANSI/AAMI ES:60601-1:2005/A2:2010
- ·IEC 60601-1-3 Edition 2.1 2013-04
- •IEC 60601-2-28:2017, Part 2-28
IEC 60601-2-54:2018, Part 2-54
•IEC 60601-1-2:2014
Bench Testing Summary
The verification test results showed compliance with the above standards. Validation was performed for overall operation by taking and reviewing test
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images. The non-clinical tests demonstrate that the device is as safe, as effective, and performs as well as the primary predicate.
Summary of Clinical Tests:
The subject of this premarket submission, did not require clinical studies to support substantial equivalence.
Conclusion:
The conclusions drawn from the nonclinical tests demonstrate that the subject device, Heart5R-110, Heart3R-110 Portable X-ray Machine is substantially equivalent to the predicate devices.
§ 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.