# K911806: Magnetic Resonance Diagnostic Accessory

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: Jun 28, 1991 after 66 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.
68 later devices descend from it; 3 cite it directly.
0 of 69 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
- K980157: Premier 7000 CTL Spine Coil (1998), 65 descendants of its own
- K994345: Magna 5000 Phased Array CTL Spine Coil (2000), 51 descendants of its own
- K042236: G-SCAN (2004), 45 descendants of its own
- K060956: G-Scan-Model 9800020000, E-Scan Model 9800010000 and E-Scan XQ-Models-9800010011/9800010005,9800010009/9800010004 (2006), 43 descendants of its own
- K063207: S-Scan Mri System (2006), 34 descendants of its own

Source page: https://510kreport.com/device/K911806
Methodology: https://510kreport.com/methodology