# K063006: GE Logiq Works

- Pathway: 510(k) (Special)
- Applicant: General Electric Co.
- Decided: Nov 2, 2006 after 31 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: 5 generations back to K842308 (1984). 15 ancestors in all.
No later device cites it as a predicate yet.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K963699: Belray/Model 096, Dental Intraoral X-Ray, Belmont Equipment Corp. (1996) Summary page 1.
- K981217: Platinum Reading, Review & Analysis Workstation, GE Medical Systems (1998) Summary page 1.
- K023557: Centricity Pacs Plus, GE Medical Systems (2002) Summary page 1.
- K042525: Centricity Radiology RA600/Centricity Cardiology CA1000/Centricity Digital Hardcopy Workstation, Ge Medical Systems Information Technologies (2004) Summary page 1.

## Indications for use
To retrieve and display for reading, diagnostic review, analysis and measurement of digital medical images acquired from DICOM compliant acquisition systems such as CT, MR, PET, X-ray and Ultrasound. Also, for images acquired from GE LOGIQ ultrasound, to process, analyze and manipulate images with the same post acquisition capability as that provided on the GE LOGIQ ultrasound scanner.

Source page: https://510kreport.com/device/K063006
Methodology: https://510kreport.com/methodology