# K945828: Echo Planar Imaging I

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems (Cleveland), Inc.
- Decided: Apr 12, 1995 after 134 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.
19 later devices descend from it; 1 cites it directly.
0 of 20 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
- K954646: Epi-II System Option W/High Performance Gradients (1996), 18 descendants of its own
- K964626: Edge/Vista System Enhancement Package (1997), 15 descendants of its own
- K974844: Outlook System Enhancement Package (1998), 11 descendants of its own
- K013858: Infinion 0.6T MR Imaging System (2002), 5 descendants of its own
- K024042: Panorama Enhancements (2003), 4 descendants of its own

Source page: https://510kreport.com/device/K945828
Methodology: https://510kreport.com/methodology