# K010509: Cedars-Sinai BPGS and Moco

- Pathway: 510(k) (Traditional)
- Applicant: Smv America
- Decided: Apr 27, 2001 after 65 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.
11 later devices descend from it; 4 cite 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- 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
- K100838: Ergo Imaging System (2010), 2 descendants of its own
- K082368: Cardius-1, -2, -3, and Cardius 1,2,3 Xpo Spect Imaging Systems, 2020TC Spect Imaging System (2008), 1 descendant of its own

Source page: https://510kreport.com/device/K010509
Methodology: https://510kreport.com/methodology