# K010571: Adc QS/Ipd Workstation

- Pathway: 510(k) (Special)
- Applicant: Agfa Corp.
- Decided: Mar 28, 2001 after 30 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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
- K063421: DX-SI (2006), 6 descendants of its own
- K072010: Quantum Direx System (2007), 5 descendants of its own
- K080905: Quantum/ Canon Cxdi Integration System, Model QG-Dig-Cxdi (2008), 4 descendants of its own
- K193574: Q-Rad System (2020), 3 descendants of its own
- K201373: DRX-Compass (2020), 2 descendants of its own

## Recalls of this device
- Nov 18, 2005 · Not classified · Z-0353-06: Users of affected systems may experience one or more of four (4) problems the clinical impact could be a loss of image(s), the need to repeat the imaging procedure and, possibly, a short delay in diag

Source page: https://510kreport.com/device/K010571
Methodology: https://510kreport.com/methodology