FDA UDI In Commercial Distribution 🇺🇸 United States

cmAngio

DI: 00860006442682 · Model: V1.0 · Curemetrix, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
cmAngio
Primary DI
00860006442682
Version / Model
V1.0
Company Name
Curemetrix, Inc.
Labeler DUNS
080081187
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-31
Public Version
2
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
08658cbe-015a-454f-a9e2-da648444ef64

Device Description

cmAngio is intended to process screening mammograms to aid a qualified interpreting physician in the current manual process of identifying Breast Arterial Calcification (BAC). cmAngio, a proprietary artificial intelligence (AI) based software, is intended to detect, at the study and breast level, the presence or absence of Breast Arterial Calcifications (BAC), an incidental finding in both Full Field Digital Mammogram (FFDM) and Digital Breast Tomosynthesis (DBT) screening mammograms. The device also marks BAC segments on thumbnails of images for localization of BAC. The software is intended to be used by qualified interpreting physicians in parallel with breast screening mammography workflow. The device is not intended for primary interpretation of digital mammography images as used for breast cancer detection and should not be used alone to make any diagnosis and/or treatment decisions. cmAngio is for prescription use only.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QIH Automated Radiological Image Processing Software

GMDN Terms

Code Name
57812 Radiology DICOM image processing application software

Identifiers

Type ID
Primary 00860006442682

Premarket Submissions

Submission Number Supplement Number
K232367 000