# K933659: Model #100GE1500 Lower Extrem Quad Detect Array Coil

- Pathway: 510(k) (Traditional)
- Applicant: Medic, Inc.
- Decided: Nov 22, 1993 after 118 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.
11 later devices descend from it; 1 cites it directly.
0 of 12 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
- K022395: 1.5T Scanmed PV Array (2002), 10 descendants of its own
- K140606: 1.5T Procure Array Coil, 3.0T Procure Array Coil (2014), 9 descendants of its own
- K142755: Siemens 3.0 Blanket Array Coil (2014), 7 descendants of its own
- K173446: Contour 24 (2017), 6 descendants of its own
- K183111: Contour 24 (2018), 3 descendants of its own

Source page: https://510kreport.com/device/K933659
Methodology: https://510kreport.com/methodology