# K151850: McKesson Cardiology

- Pathway: 510(k) (Traditional)
- Applicant: Mckesson Israel, Ltd.
- Decided: Aug 11, 2015 after 35 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: 7 generations back to K842308 (1984). 34 ancestors in all.
2 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)
- K112720: Mckesson Horizon Cardiology, Mckesson Israel, Ltd. (2012) Summary page 4.
- K112570: Centricity Cardio Imaging, Ge Healthcare Integrated IT Solutions (2011) Summary page 4.

## Most influential descendants
- K181080: McKesson Cardiology (2018), 1 descendant of its own
- K212528: Change Healthcare Cardiology (2021), 0 descendants of its own

## Indications for use
McKesson Cardiology™ is an integrated multimodality image and information system designed to perform the necessary functions required for import, export, storage, archival, review, analysis, quantification, reporting and database management of digital cardiovascular images and information from other data sources. McKesson Cardiology™ is intended for use in the Cardiology, Radiology or other departments throughout the healthcare facility and distributed locations and may be part of a larger PACS configuration. McKesson Cardiology™ offers support for third-party plug-ins in order to enable the use of commercially available tools for analysis, quantification and reporting. McKesson Cardiology™ is intended to assist trained professionals in the viewing and diagnostic interpretation of images and other information for the diagnosis and treatment of cardiac and vascular disease.

Source page: https://510kreport.com/device/K151850
Methodology: https://510kreport.com/methodology