# K003264: QPS/BPGS/Moco Processing Applications for Entegra Workstation

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems F.I. Haifa
- Decided: Dec 21, 2000 after 64 days
- Product code: KPS (System, Tomography, Computed, Emission)
- Device class: 2
- Regulation: 21 CFR 892.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
25 later devices descend from it; 4 cite it directly.
0 of 26 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
- K110507: Cardiac Scanner and Processing System (2011), 9 descendants of its own
- K023110: Cedars-Sinai Motion Correction (Moco) Software, Model 111005 (2002), 9 descendants of its own
- K052430: Cardius-1, Cardius-2, Cardius-3, 2020TC Spect Imaging System (2005), 7 descendants of its own
- K070542: Cardius 1, 2 and 3 Xpo and 2020TC Spect Imaging Systems (2007), 6 descendants of its own
- K161740: D-SPECT Scanner, D-SPECT L Scanner (2016), 5 descendants of its own

Source page: https://510kreport.com/device/K003264
Methodology: https://510kreport.com/methodology