# K140606: 1.5T Procure Array Coil, 3.0T Procure Array Coil

- Pathway: 510(k) (Special)
- Applicant: Resonance Innovations, LLC
- Decided: May 12, 2014 after 63 days
- Product code: MOS (Coil, Magnetic Resonance, Specialty)
- 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
Longest line of descent: 2 generations back to K933659 (1993). 2 ancestors in all.
9 later devices descend from it; 2 cite 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)
- K022395: 1.5T Scanmed PV Array, Medic, Inc. (2002) Summary page 1.

## Most influential descendants
- 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
- K223429: Contour Knee (2023), 2 descendants of its own
- K193140: Flex Body SPEEDER (2020), 1 descendant of its own

## Indications for use
The coil is indicated for use by the order of a physician to be used as an accessory to a General Electric 1.5T or 3.0T magnetic resonance scanner for general human anatomy imaging as supported by the scanner. These images, when interpreted by a trained physician, may assist in medical diagnosis.

Source page: https://510kreport.com/device/K140606
Methodology: https://510kreport.com/methodology