# K913475: Magnetic Resonance Diagnostic Device

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Oct 30, 1991 after 86 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.
181 later devices descend from it; 1 cites it directly.
2 of 182 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K960265: Advantage Windows with Functool Option (1996), 180 descendants of its own
- K971965: Philips Easyvision (1998), 74 descendants of its own
- K022292: Impax Diagnostic Display Station,Impax Clinical Review Station,Impax for Cardiology Clinical Review Satation,Impax Ortho (2002), 48 descendants of its own
- K110573: Ready View (2011), 38 descendants of its own
- K061429: Dynamic Mri Software Option for C-Scan, E-Scan XQ and E-Scan Opera (2006), 32 descendants of its own

Source page: https://510kreport.com/device/K913475
Methodology: https://510kreport.com/methodology