K Number
K192098
Device Name
EzMobile
Manufacturer
Date Cleared
2020-01-20

(168 days)

Product Code
Regulation Number
892.2050
Panel
RA
Reference & Predicate Devices
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

EzMobile is dental imaging software that is intended to provide various tools for maxillofacial radiographic imaging. These tools are available to view a series of DICOM compliant dental radiology images and are meant to be used by trained medical professionals such as radiologist and dentist. EzMobile is intended for use as software to acquire, view and save 2D image files, load DICOM project files from panorama, cephalometric, and intra-oral imaging equipment.

Device Description

EzMobile is dental imaging software that is intended to provide various tools for maxillofacial radiographic imaging. These tools are available to view a series of DICOM compliant dental radiology images and are meant to be used by trained medical professionals such as radiologist and dentist. EzMobile is intended for use as software to acquire, view and save 2D image files, load DICOM project files from panorama, cephalometric, and intra-oral imaging equipment.

AI/ML Overview

The provided text is an FDA 510(k) clearance letter for EzMobile, a dental imaging software. It does not contain information about acceptance criteria for a device's performance or a study proving the device meets acceptance criteria related to diagnostic accuracy or AI performance metrics.

The clearance letter primarily addresses regulatory compliance and substantial equivalence to a predicate device. The "Indications for Use" section describes the software's intended function (viewing/saving DICOM dental images, etc.) but does not specify performance metrics or a study demonstrating their achievement.

Therefore,Based on the provided document alone, I cannot provide the requested information regarding the acceptance criteria and the study that proves the device meets them. The document is an FDA clearance letter focusing on regulatory compliance and substantial equivalence, not a performance study report.

§ 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).