# K923264: General Purpose Flex Coil

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: Sep 30, 1992 after 90 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.
6 later devices descend from it; 2 cite it directly.
0 of 7 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
- K030953: GE 3.0T General Purpose Flex Coil (2003), 4 descendants of its own
- K061715: Mrgfus General Purpose and Breast Coil (2006), 2 descendants of its own
- K083434: TT1 General Purpose Coil (2008), 1 descendant of its own
- K123681: 1.5T 4CH Large Flex Coil, 1.5 4CH Small Flex Coil (2013), 0 descendants of its own
- K113280: Carotid Coil GE 1.5T (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K923264
Methodology: https://510kreport.com/methodology