# K182750: 4D View

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems Ultrasound and Primary Care Diagnostics
- Decided: Dec 21, 2018 after 84 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K935595 (1995). 104 ancestors in all.
No later device cites it as a predicate yet.
0 of 105 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131118: 4D VIEW, GE Healthcare (2013) Summary page 4.

## Indications for use
Image display of GE Ultrasound 3D/4D data sets for diagnostic purposes including measurements on displayed image.

Source page: https://510kreport.com/device/K182750
Methodology: https://510kreport.com/methodology