# K000315: Ventricular Analysis Toolkit Option

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Mar 27, 2000 after 55 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
450 later devices descend from it; 1 cites it directly.
1 of 451 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K013422: Cardiq Function (2001), 449 descendants of its own
- K041267: Cardiq Analysis Iii (2004), 331 descendants of its own
- K052029: Syngo Circulation (2005), 296 descendants of its own
- K063762: Syngo Circulation Software Package with Extended Functionality (2007), 263 descendants of its own
- K091373: Syngo Trued (2009), 200 descendants of its own

Source page: https://510kreport.com/device/K000315
Methodology: https://510kreport.com/methodology