(15 days)
The Anythink is a medical image processing system, which offers comprehensive solutions to viewing, manipulation, communication and storage of multi-modality DICOM images and data on exchange media.
The Anythink® is a universal imaging platform, and supports different modalities, but it is not intended for the displaying of digital mammography images for diagnosis in the U.S.
The Anythink® is based on Windows XP, providing a set of software solutions with flexible configurations in accordance with different medical imaging missions and demands. The system accepts multi-modality DICOM images and allows for view, post-processing, and communication. This product is not intended for use with or for the primary diagnostic interpretation of mammography images in the U.S.
Due to specific customer requirements and the clinical focus, the Anythink® consists of two parts: Basic Functions and Optional Functions.
Basic functions are mandatory, allowing view, easy manipulation, storage and communication of DICOM formatted images, except in the case of mammography images. Management of patient information is also included.
Optional Functions are a set of professional image processing functions, designed for specific modalities. Depending on the precise requirement, customers can select the appropriate function(s) from the optional functions, under the precondition of installing Basic Functions.
The clinician retains the ultimate responsibility for making the pertinent diagnosis based on their standard practices. The Anythink® is intended to assist the physician in diagnosis or treatment planning.
The provided FDA 510(k) summary for the Anythink® / Anythink PACS Workstation (K131299) establishes substantial equivalence to a predicate device (Siemens Syngo Multimodality Workplace, K072728). However, this summary does not include a study that explicitly proves the device meets specific acceptance criteria based on quantitative performance metrics, such as sensitivity, specificity, or reader performance.
Instead, the submission relies on a comparison of technological characteristics and intended use to demonstrate substantial equivalence. For medical image processing systems like PACS workstations, the FDA often accepts this approach without requiring a full-scale clinical performance study if the new device shares fundamental technological characteristics and intended use with a legally marketed predicate.
Therefore, many of the requested details about acceptance criteria, study design, sample size, ground truth, and reader studies are not present in this 510(k) summary. This is typical for Class II medical devices considered substantially equivalent, where the focus is on demonstrating that the new device does not raise new questions of safety and effectiveness compared to an existing one.
However, I can extract information related to the device's technical specifications and general safety and effectiveness claims.
Here's a breakdown of what can be inferred or explicitly stated based on the provided text, and what information is missing:
1. Table of Acceptance Criteria and Reported Device Performance
This document does not present a table of quantitative acceptance criteria (e.g., minimum accuracy, sensitivity, or specificity) or numerical performance metrics for the Anythink® PACS Workstation. The "acceptance criteria" for a 510(k) submission are fundamentally about demonstrating substantial equivalence, meaning the device is as safe and effective as a predicate device. The performance is largely implied to be equivalent to the predicate through the comparative analysis of features.
The document mainly focuses on comparing the functions of the Anythink® with the Siemens Syngo-Multimodality Workplace:
| Function | Anythink Description | Predicate (Siemens Syngo) Description |
|---|---|---|
| Hardware requirement | CPU: Dual-core 2.8G, Hard disk: 250G, Memory: 4 GB, Monitor: 19 inch LCD (1280x1024), Video card: Nvidia serial (1G), DVD-RW, Keyboard/Mouse, 100M/1000M network card | Type: FSC Celsius R640, Processor: 2 x 3.0 GHz Intel Xeon Dual core, RAM: 4 GB (upgradable to 12 GB), System disk: 73 GB, Hard disk for image data: 147 GB, DVD writer, DVD reader, Floppy disk, Graphics card: OpenGL, Network: 2 x Gigabit Ethernet LAN, Monitors: Flat-screen color/monochrome |
| Operating system | Microsoft Windows XP | Windows XP |
| Patient information management | Creating new, editing, deleting patient info; inquires and ranks patient info; disk backup; burns data to DICOM, AVI, MPEG. | Offers consistent access to patient and exam data from all applications. DICOM Media Storage for data exchange on CD/DVD. |
| Image Browsing | Adjusting windows width/level by hotkeys, presetting tools, or manually; single/multiple window display, switching images within/among series, between patients. | Comprehensive functions for 2D processing and image evaluation; Multimodality display with intuitive tools; Display and arrange images to suit diagnostic task. |
| Image Manipulation | Applies to DICOM compliant images (except digital mammography); adjusts for different human tissue/body positions; positive-negative conversion, local/overall zoom, dying scheme, flip, rotate, edge enhancement/smoothing, measurement, annotation. | Review, process, evaluate results, prepare for supporting physician's diagnosis. Send to syngo Filming, store, or send to other hospital locations. |
| Image Transmit | Applies to DICOM compliant images (except digital mammography); supports image transformation between system and other DICOM devices; input images from disk to system. | DICOM functions for receiving/sending digital examinations and local data exchange; connecting to radiological network. |
| Image Storage | Six image/series storage functions; saving current image to temporary area/clipboard/file/database; saving current sequence as video file or to database. Applicable for DICOM compliant images (except digital mammography). | DICOM Storage for data transfer/archiving; DICOM Storage Commitment; DICOM Query & Retrieve; DICOM Print. |
| 3D reconstruction (3D View) | MPR, Max/Min Intensity projection (MIP), Shaded surface Display, Volume Rendering, Virtual Endoscopy for CT/MRI images; 3D display of various tissues, bone, angiosteosis, etc. | Processes volume datasets (MIP, MPR, SSD); Displays CT, MR, NM, XA volume with editing (e.g., bone removal); Volume Rendering Technique. |
| XA heart and coronary artery analysis (QCA, LVA) | QCA: Applicable for XA coronary artery projection, vessel stenosis analysis (Live-wire algorithm). LVA: For XA heart projection, analysis of cardiac ejection functional and wall motion (radial/center line method). | syngo Angio (DSA): Shifts DSA image processing. syngo QCA: Quantitative coronary vessel analysis. syngo LVA: Left ventricle analysis (ejection fraction, wall motion). syngo LVA biplane: For simultaneous biplane acquisitions. syngo QVA: Quantitative vessel analysis for abdominal/peripheral vessels. |
| CT Coronary Artery Analysis | Extracting/adjusting coronary artery tree in CTA, single coronary artery vessel and analysis in 3D (QCA method). | syngo Circulation: Comprehensive cardiac/chest pain evaluation with reporting. syngo Circulation QCA with Plaque Analysis: Fast coronary tree segmentation, stenosis quantification, stent planning, plaque analysis. syngo Circulation LVA: Complete ventricular function evaluation in multiphase cardiac datasets. |
| Virtual Colonoscopy | Assistant tool for detecting colonic lesions from CT images (extracting colon image, endoluminal display, marking suspected lesions). Applies VR+SSD. | syngo Colonography: Locates/evaluates colon polyps using non-invasive, real-time virtual 3D endoluminal viewing. syngo Colonography Polyp Enhanced Viewing (PEV): Automated second reader tool. syngo Colonography Unfolding: Allows unfolding colon for easier polyp visualization. |
| 3D Angiostenosis analysis (syngo IC3D) | Creates 3D models of coronary vessel segments from two projection images for image analysis and stent indications; quantitative analysis of vessel. | Creates 3D models of coronary vessel segments for highly accurate quantification of lesions - stent size and length quantification with as few as two projection images. |
2. Sample Size Used for the Test Set and Data Provenance
- Sample Size: Not specified. The submission does not detail a specific test set of medical cases used for performance evaluation in the traditional sense (e.g., a cohort of patients/studies).
- Data Provenance: Not specified. Since no specific test set study is presented, the country of origin or whether the data was retrospective or prospective is not mentioned. The device's intended market is the U.S.
3. Number of Experts Used to Establish Ground Truth and Qualifications
- Number of Experts: Not specified. As there's no described performance study with ground truth establishment, this information is not provided.
- Qualifications of Experts: Not specified.
4. Adjudication Method for the Test Set
- Adjudication Method: Not applicable. No study with an adjudication process is described in this summary.
5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study Was Done
- MRMC Study: No. This type of study (comparing human readers with and without AI assistance) is not mentioned. The device is a PACS workstation, not an AI-assisted diagnostic tool in the sense of providing specific lesion detection or characterization beyond standard viewing and manipulation functions. The comparative effectiveness is implicitly demonstrated by comparing the functionalities and technical characteristics to the predicate, not by a human-in-the-loop study.
- Effect Size: Not applicable as no MRMC study was performed.
6. If a Standalone (Algorithm Only) Performance Study Was Done
- Standalone Study: No. The device is a PACS workstation, which is a tool for viewing and manipulating images, not a standalone diagnostic algorithm that would generate outputs independent of a human operator. Its performance is based on its functionality and ability to process and display images robustly, not on an "algorithm only" diagnostic accuracy.
7. The Type of Ground Truth Used
- Type of Ground Truth: Not applicable. Since no performance study measuring diagnostic accuracy against a ground truth is described, this information is not provided. The "ground truth" for a PACS workstation primarily relates to its ability to accurately and reliably display and process DICOM images according to established standards.
8. The Sample Size for the Training Set
- Sample Size: Not applicable/Not specified. The device is a software solution with "Basic Functions" and "Optional Functions" designed for image processing. It's not described as a deep learning or machine learning system that would require a large training set in the typical sense for algorithms that learn patterns for diagnostic tasks. Its development likely involved standard software engineering validation and verification processes rather than data-driven model training.
9. How the Ground Truth for the Training Set Was Established
- Ground Truth Establishment: Not applicable/Not specified. As there's no mention of a training set for a machine learning model, the method for establishing its "ground truth" is not relevant or provided in this document.
In conclusion:
The provided 510(k) summary for the Anythink® PACS Workstation demonstrates substantial equivalence primarily through a comparison of functional and technical characteristics with a legally marketed predicate device, the Siemens Syngo Multimodality Workplace. It does not present quantitative performance data from a clinical study, involve specific test sets of patient cases, or refer to machine learning model training/evaluation, which are common for AI/ML-based diagnostic devices today. The "acceptance criteria" here are met by demonstrating that the new device performs its intended functions (viewing, manipulation, communication, storage of DICOM images) reliably and does not raise new issues of safety or effectiveness compared to the predicate.
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K131299
Page 1 of 11
510K Summary of safety and effectiveness
MAY 2 2 2013
This summary of 510(K) safety and effectiveness information is submitted in accordance with the requirements of 21 CFR Part 807.92
1. GENERAL INFORMATION
| Establishment: | Beijing Crealife Technology Co., Ltd. |
|---|---|
| Address: | Room 519, Huitong Office BuildingB20 Fuxing Road, Haidian DistrictBeijing, China 100036 |
| Registration Number: | 3006104453 |
| Contact Person: | Weihua ZhouManagement RepresentativeTelephone:(0086)1088288713-6200Fax: (0086)1088112709Mobile :(0086)1013683004936 |
Date of Preparation of Summary: Jan. 16, 2013
| Device Name: | |
|---|---|
| ·Trade Name: | Anythink® / Anythink PACS Workstation |
| Classification: | Picture Archiving and Communication System |
| Classification Panel: | Radiology |
| CRF Section: | 21 CFR§892.2050 |
| ·Device Class: | Class II |
| ·Product Code: | LLZ |
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SAFETY AND EFFECTIVENESS INFORMATION SUPPORTING THE 2. SUBSTANTIAL EQUIVALENCE DETERMINATION
·Intended Use:
The Anythink is a medical image processing system, which offers comprehensive solutions to viewing, manipulation, communication and storage of multi-modality DICOM images and data on exchange media.
.
The Anythink® is a universal imaging platform, and supports different modalities, but it is not intended for the displaying of digital mammography images for diagnosis in the U.S.
· Device Description
The Anythink® is based on Windows XP, providing a set of software solutions with flexible configurations in accordance with different medical imaging missions and demands. The system accepts multi-modality DICOM images and allows for view, post-processing, and communication. This product is not intended for use with or for the primary diagnostic interpretation of mammography images in the U.S.
Due to specific customer requirements and the clinical focus, the Anythink® consists of two parts: Basic Functions and Optional Functions.
Basic functions are mandatory, allowing view, easy manipulation, storage and communication of DICOM formatted images, except in the case of mammography images. Management of patient information is also included.
Optional Functions are a set of professional image processing functions, designed for specific modalities. Depending on the precise requirement, customers can select the appropriate function(s) from the optional functions, under the precondition of installing Basic Functions.
The clinician retains the ultimate responsibility for making the pertinent diagnosis
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based on their standard practices. The Anythink® is intended to assist the physician in diagnosis or treatment planning.
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· Technological characteristics
The Anythink® will be marketed as a software solution for the end user (with recommended hardware requirements). It will be installed by Crealife's service engineers. The Anythink® described supports DICOM formatted images, and the system is based on the Windows XP operating system.
· General Safety and effectiveness concerns
The Anythink® software is specified, validated and tested under a registered ISO13485 and 21 CFR Part820 compliant Quality System.
The device labeling contains instructions for use and any necessary cautions and warnings, to provide for safe and effective use of the device.
Risk Management is ensured via a Risk Analysis, which is used to identify potential hazards. These potential hazards are controlled via software development, verification and validation testing.
· Substantial Equivalence
The Anythink®, addressed in this premarket notification, is substantially equivalent to the following commercially available devices:
| 510K Number | Trade or Model Name | Manufacturer |
|---|---|---|
| K072728 | Syngo Multimodality Workplace | Siemens AG MedicalSolutions |
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| Function | Anythink | Description | Function | SIEMENS Syngo-Multimodality Workplace | Description | ||
|---|---|---|---|---|---|---|---|
| Hardwarerequirement | CPU: Dual-core 2.8GHard disk: 250GMemory: 4 GBMonitor Driver: 19 inch LCDThe resolution is no less than 1280*1024Video card: Nvidia serial video card, 1G video memory | Hardwarerequirement | Type: FSC Celsius R640Processor: 2 x 3.0 GHz Intel Xeon Dual coreRAM: 4 GB (upgradable to 12 GB)System disk: 73 GBHard disk for image data: 147 GBDVD writer: DVD-R, CD-RDVD reader: DVD-ROM, CD-ROMFloppy disk: 3,5", 1,4 MBGraphics card: OpenGL graphicsNetwork: 2 x Gigabit Ethernet LAN on boardMonitors: Flat-screen color monitor, high end 19" and/or Flat screen monochrome monitor, high end | ||||
| CD Drive: DVD-RWInput Device: Keyboard/Mouse100M/1000M network card | |||||||
| Operatingsystem | Microsoft Windows XP | Operatingsystem | Windows XP | Offers consistent access to patient and exam data from all applications. | |||
| Patientinformationmanagement | Provides creating new, editing and deleting patient information and other management functions, inquires and ranks patient information using key words; provides disk backup function and burns data to DICOM, AVI or MPEG format. | ArchivingandNetworking | DICOM Media Storage for data exchange on CD and DVD media. | Applicable for medical images from DICOM compliant sources, except digital mammography. |
Technological characteristics comparison of the Anythink and predicate devices
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| Function | AnythinkDescription | Function | SIEMENS Syngo-Multimodality WorkplaceDescription |
|---|---|---|---|
| ImageBrowsing | Supports adjusting windows width/level byhotkeys, presetting tools or manually;single/multiple window display, switching imageswithin one series as well as among different series.Image switching between various patients is alsoavailable. | syngoViewing | Offers comprehensive functions for 2D processingand image evaluation.Multimodality display with a wide range of intuitivetools.Display and arrange the images in the way bestsuited to the diagnostic task. |
| ImageManipulation | Applicable for medical images from DICOMcompliant sources, except digital mammography,can apply to image adjustment of different humantissue, body position, to meet the requirements ofreading images.Provides converting positive-negative image,local/overall zoom, dying scheme, image flip(vertical/horizontal), image rotate (+/- 90 degree);image edge enhancement/ smoothing, imagemeasurement and annotation. | Review, process and evaluate the results and preparethem for supporting physician's diagnosis.Send the images to syngo Filming, store them, orsend them to other locations in the hospital: | |
| ImageTransmit | Applicable for medical images from DICOMcompliant sources, except digital mammography.Supports image transformation between the systemand other DICOM devices and can input imagesfrom disk to system; | ArchivingandNetworking | syngo offers DICOM functions such as receivingand sending digital examinations and local dataexchange to media like CD-R or DVD as well asconnecting the syngo MultiModality Workplace tothe radiological network.. |
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| Function | Anythink | Description | Function | SIEMENS Syngo-Multimodality Workplace | Description |
|---|---|---|---|---|---|
| Image Storage | Provides six image/series storage function, allows saving current image to temporary area/clipboard/file/database, saving current image sequence as video file or back to database.Applicable for medical images from DICOM compliant sources, except digital mammography. | DICOM Storage for data transfer and archiving to connected network nodesDICOM Storage Commitment to confirm successful storage at destinationDICOM Query & Retrieve to search and access patient data on connected DICOM nodesDICOM Print for documentation of images on DICOM-capable laser cameras and network printers | |||
| / | 3DBasic | Processes volume datasets from various modalities as MIP, MPR, or SSD reformats, quickly and easily in routine use. | |||
| 3D reconstruction (3D View) | Multiplanar Reconstruction MPR: Applicable for CT or MRI image, used for the 3D displaying of various tissue;Max/Min Intensity projection MIP: Applicable for CT or MRI image, mainly used for 3D displaying of bone, angiosteosis and other high density tissue;Shaded surface Display: Applicable for CT or MRI image, used for 3D display of bone, lung and other tissues;Volume Rendering: Applicable for CT or MRI image, used for 3D display of various tissue;Virtual Endoscopy: Applicable for CT or MRI image, used for 3D display internal wall of vessel and cavity | syngoVRT | Displays CT, MR, NM, and conventional angiography volume datasets with excellent quality to the finest detail and provides advanced editing and provides advanced editing, including bone removal.Volume Rendering Technique: 3D visualization of volume data.Multi-modality application for CT, MR and 3D-XA data. Provides virtual endoluminal views of hollow structures | ||
| Syngo Fly Through | |||||
| Anythink | SIEMENS Syngo-Multimodality Workplace | ||||
| Function | Description | Function | Description | ||
| Edit 3D: Applicable for observing, selecting, measuring and annotating of 3D images | XA heart and coronary artery analysis | Quantitative Coronary artery analysis(QCA): Applicable for XA coronary artery projection image, mainly used for vessel stenosis analysis, calculating stenosis rate and other relevant parameters; Functional implementation method: defined analyze-needed vessel, segmentalize vessel outline, calculate reference vessel outline, calculate stenosis analysis parameter, carry on multiple stenosis analysis; this implementation process applies Live-wire algorithm. The function is under the precondition of installing Basic Functions. | syngo Angio (DSA) | syngo Angio (DSA) | Shifts DSA image processing of native and subtracted angiography series to the syngo MultiModality Workplace - the imaging system is freed immediately for the next acquisition. |
| syngo QCA | Provides quantitative coronary vessel analysis, optimized for small vessels like coronary arteries. | ||||
| Function | Anythink | Description | SIEMENS Syngo-Multimodality Workplace | Function | Description |
| Left Ventricular functional Analysis(LVA):Applicable for XA heart projection image, mainlyused for the analysis of the cardiac ejectionfunctional and wall motion; | Function implementation method: selectend-diastolic image, define the left ventricularoutline of end-diastolic; select end-systole image,define the left ventricular outline of end-systole;input patient's height, weight; calculate ejectionfraction and other heart functional parameters;select wall movement analysis method (radial linemethod, center line method) | • syngo LVAProvides left ventricle analysis including e. g.ejection fraction calculation and wall motionanalysis. | |||
| The function is under the precondition of installingBasic Functions. | • syngo LVA biplaneProvides left ventricle analysis for simultaneousbiplane acquisitions. | ||||
| • syngo QVAProvides quantitative vessel analysis for abdominaland peripheral vessels. | |||||
| Anythink | Description | Function | SIEMENS Syngo-Multimodality Workplace | Description | |
| Applicable for CT image, mainly used for analyzing coronary artery; | Implementation method: extracting and adjusting coronary artery tree in the CTA image, define single coronary artery vessel and vessel analysis in the 3D image. This function applies QCA calculation method. | syngo Circulation | syngo Circulation | Offers comprehensive cardiac and chest pain evaluation with integrated reporting in a single application. | |
| The function is under the precondition of installing both Basic Functions and 3D View. | • syngo Circulation QCA with Plaque Analysis | ||||
| Allows fast coronary tree segmentation, accurate stenosis quantification, stent planning and plaque analysis. | |||||
| • syngo Circulation LVA | |||||
| Enables complete ventricular function evaluation in multiphase cardiac datasets. | |||||
| Applicable for CT image, an assistant tool to obtain the endoluminal view of the colon derived for the purpose to detect colonic lesions. It provides functionality for extracting colon image, endoluminal display of the colon, and marking suspected lesions.) | Implementation method: 3D panoramic view, unfolding colon and endoscope of extracting colon, analysis colon, display colon in the CTC image. Apply the VR+SSD. | syngo Colonography | syngo Colonography | Locates and evaluates colon polyps using non-invasive, real-time virtual 3D endoluminal viewing for CT datasets. | |
| The function is under the precondition of installing | • syngo Colonography Polyp Enhanced Viewing (PEV) Supports as automated second reader tool the visualization of lesions. | ||||
| • syngo Colonography Unfolding Allows the user to unfold the colon for easier polyp visualization and navigation. |
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| Description | Function | Description | |
|---|---|---|---|
| Anythink | Creates 3D models of coronary vessel segments with two projection images, providing image analysis and stent indications of 3D angiostenosis. | syngo IC3D | SIEMENS Syngo-Multimodality WorkplaceCreates 3D models of coronary vessel segments for highly accurate quantification of lesions - stent size and length quantification with as few as two projection images. |
| Applicable for XA projection image, mainly used for 3D quantitative analysis of vessel. | syngo IC3D | ||
| Implementation method: select two vessel projection image of which the angle is between 60 and 120 degree, separately define perfusion vessel's stenosis information, stenosis vessel 3D display, stenosis parameter calculation, virtual stent display; | |||
| This function is under the precondition of installing Basic Functions |
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Page 11 of 11
K131299
Crealife, Beijing
· Conclusion as to Substantial Equivalence
The Anythink®, described in this premarket notification has the same intended use and similar technical characteristics as the device listed above.
In summary, the Anythink® does not introduce new indications for use, nor does the use of the device result in any new potential safety risks. The Anythink® is substantially equivalent to and performs as well as the predicate device.
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DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/11/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three lines representing its body and wings. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" are arranged in a circular pattern around the eagle.
Public Health Service
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G60 Silver Spring, MD 20993-0002
May 22, 2013
Beijing Crealife Technology Co., Ltd. % Mr. Ned Devine Senior Staff Engineer Underwriters Laboratories, Inc. 333 Pfingsten Road NORTHBROOK IL 60062
Re: K131299
Trade/Device Name: Anythink PACS Workstation Regulation Number: 21 CFR 892.2050 Regulation Name: Picture archiving and communications system Regulatory Class: II Product Code: LLZ Dated: April 16, 2013 Received: May 07, 2013
Dear Mr. Devine:
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. Ilisting 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 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
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Page 2 - Mr. Ned Devine
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Small Manufacturers, International and Consumer Assistance at its tollfree number (800) 638 2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 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/ReportalProblem/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/MedicalDevices/ResourcesforYou/Industrv/default.htm.
Sincerely yours,
Michael D. O'Hara for
Janine M. Morris Director, Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health
Enclosure
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Indications for Use Form
K131299 510(k) Number (if known):
Device Name: _________________________________________________________________________________________________________________________________________________________________
Indications for Use:
The Anythink is a medical image processing system, which offers comprehensive solutions to viewing, manipulation, communication and storage of multi-modality DICOM images and data on exchange media.
The Anythink® is a universal imaging platform, and supports different modalities, but it is not intended for the displaying of digital mammography images for diagnosis in the U.S.
Prescription Use AND/OR Over-the-Counter Use --------(Part 21 CFR 801 Subpart D) .(21 CFR 801 Subpart C)
(Please do not write below this line - continue on another page if needed)
Concurrence of the CDRH, Office of In Vitro Diagnostics and Radiological
Health (OIR)
Machiel D. D'Hara
(Division Sign-Off)
Office of In Vitro Diagnostics and Radiological Health
K131299 ·
510(k) Number
Page 1 of 1
§ 892.2050 Medical image management and processing system.
(a)
Identification. A medical image management and processing system is a device that provides one or more capabilities relating to the review and digital processing of medical images for the purposes of interpretation by a trained practitioner of disease detection, diagnosis, or patient management. The software components may provide advanced or complex image processing functions for image manipulation, enhancement, or quantification that are intended for use in the interpretation and analysis of medical images. Advanced image manipulation functions may include image segmentation, multimodality image registration, or 3D visualization. Complex quantitative functions may include semi-automated measurements or time-series measurements.(b)
Classification. Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern).