AccessGUDID - DEVICE: ClariCT.AI (08800046800211)

GUDID

Device Identifier (DI) Information

Brand Name: ClariCT.AI
Version or Model: ClariCT.ACE
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: ClariPI Inc.

Primary DI Number: 08800046800211
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 693744312 *Terms of Use

Device Description: ClariCT.AI, is a software device intended for networking, communication, processing and enhancement of CT images in DICOM format regardless of the manufacturer of CT scanner or model. The original cleared device (K183460) is a software application to denoise on CT images, integrated with the clinical environment through DICOM communication on an on-premise environment, and runs under Microsoft Windows platform. The device consists of Denoise Processing module that denoises CT images and other modules (Window application module) that provide many features such as handling DICOM connection from/to PACS, user interface, worklist management and viewer. The subject device, ClariCT.AI, has added a new module (named Al Marketplace Integration module) to the original cleared device (K183460) to enable installation on the Al Marketplace system. The module integrates the Denoising Processor of original device into the Al Marketplace system and includes an optional ACE module that additionally improves the CNR of CECT (Contrast-Enhanced CT) images.ClariCT.AI, consists only of the Al Marketplace Integration Module and the Denoising Processor, can be installed in the Al Marketplace system that integrates centrally with PACS and seamlessly integrates into the existing IT and modality infrastructure. An Al Marketplace system, which can be integrated with the ClariCT.AI, is a cloud-based Al platform service that connects end users (e.g. hospitals, imaging centers) and Al medical imaging applications developed by third parties. These Al Marketplace systems provide many features such as handling DICOM connection from/to PACS, user interface, authentication, worklist control, and orchestrating third party Al applications. With the newly added module, ClariCT.Al will function as a software device integrated with such system, and therefore the responsibility of our software is bound to change so as to take care of only essential functionality such as denoising process and system interfa

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
57812	Radiology DICOM image processing application software	A software application intended to facilitate management, distribution, and/or viewing of radiological digital imaging and communications in medicine (DICOM) image data; it is not intended for pathological image interpretation (i.e., not intended to detect and localize suspected abnormalities). It may be intended to facilitate image management (e.g., viewing, communication, printing, recording/disc burning) and/or image quality manipulation and quantification (e.g., non-interpretive graphical overlays).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LLZ	System, Image Processing, Radiological

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K212074	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 1b15f5bb-2c5f-4d62-98c6-67a4b48e0ed8
Public Version Date: December 05, 2024
Public Version Number: 1
DI Record Publish Date: November 27, 2024