# K924605: Magnetic Resonance Diagnostic Accessory

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: May 21, 1993 after 252 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.
76 later devices descend from it; 3 cite it directly.
0 of 77 devices in its family (counting itself) have 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
- K994282: Mri- Flow Analytical Software Package (2000), 73 descendants of its own
- K031927: GE Delta Software Option for Mri (2003), 22 descendants of its own
- K121762: Cardiac VX (2013), 21 descendants of its own
- K091262: MR Cardiac Function Analysis (2009), 21 descendants of its own
- K103465: Synapse 3D Cardiac Tools (2011), 20 descendants of its own

Source page: https://510kreport.com/device/K924605
Methodology: https://510kreport.com/methodology