# K022395: 1.5T Scanmed PV Array

- Pathway: 510(k) (Special)
- Applicant: Medic, Inc.
- Decided: Aug 13, 2002 after 21 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: 1 generation back to K933659 (1993). 1 ancestor in all.
10 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)
- K933659: Model #100GE1500 Lower Extrem Quad Detect Array Coil, Medic, Inc. (1993) Summary page 1.

## Most influential descendants
- 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
- K223429: Contour Knee (2023), 2 descendants of its own

## Indications for use
Soft tissue and bone imaging of both lower extremities simultaneously as allowed by the MRI system. Magnetic resonance peripheral angiography.

Source page: https://510kreport.com/device/K022395
Methodology: https://510kreport.com/methodology