# K110071: Cor Analyzer

- Pathway: 510(k) (Special)
- Applicant: Rcadia Medical Imaging, Ltd.
- Decided: Jan 31, 2011 after 21 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K913770 (1991). 32 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 37 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072242: Cor Analyzer II, Model V1.7, Rcadia Medical Imaging, Ltd. (2007) Summary page 1.

## Most influential descendants
- K123646: Emory Cardiac Toolbox 4.0 (2013), 3 descendants of its own
- K231731: Optional Screen Displays for HeartSee Cardiac P.E.T. Processing Software - HeartSee version 4 (2023), 1 descendant of its own
- K243881: HeartSee™ Cardiac P.E.T. Processing Software For Myocardial Perfusion and Coronary Flow Reserve (CFR) Version 4 (2025), 0 descendants of its own
- K223422: Emory Cardiac Toolbox 4.3 (2023), 0 descendants of its own

## Indications for use
The COR Analyzer is intended to assist a trained physician to analyze Computed Tomography (CT) Angiographic images. The device is not intended for use with mammography. The COR Analyzer is specifically indicated to provide visualization of the major coronary vesseis and lesions, thus assisting the physician in visualizing the coronary anatomy and pathology. COR Analyzer has abilities for coronary vessels segmentations, abnormalities display and processing.

Source page: https://510kreport.com/device/K110071
Methodology: https://510kreport.com/methodology