# K002936: Modification to IDS5 Image Display System

- Pathway: 510(k) (Special)
- Applicant: Sectra-Imtec AB
- Decided: Oct 17, 2000 after 26 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
No predicates in its family tree.
436 later devices descend from it; 4 cite it directly.
1 of 437 devices in its family (counting itself) has 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
- K022881: Cedara I-Softview (2002), 413 descendants of its own
- K040468: Cedara I-Softview and Cedara I-Readmammo (2004), 255 descendants of its own
- K053301: Cedara I-Response Cedara Pet/CT (2006), 221 descendants of its own
- K071950: Syngo Trued (2007), 201 descendants of its own
- K091373: Syngo Trued (2009), 200 descendants of its own

Source page: https://510kreport.com/device/K002936
Methodology: https://510kreport.com/methodology