# K050196: Sectra IDS5 Workstation

- Pathway: 510(k) (Special)
- Applicant: Sectra Imtec AB
- Decided: Feb 24, 2005 after 28 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: 2 generations back to K033712 (2003). 2 ancestors in all.
36 later devices descend from it; 3 cite it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040376: Sectra IDS5 Radiology Workstation; Sectra MPR Package; Sectra 3D Package, Sectra-Imtec AB (2004) Summary page 1.

## Most influential descendants
- K051315: Modification to: Sectra IDS5 Workstation (2005), 35 descendants of its own
- K063093: Sectra Workstation, Version 11.1 (2006), 34 descendants of its own
- K073272: Workstationone Breast Imaging Workstation (2007), 27 descendants of its own
- K082483: Quantra (2008), 25 descendants of its own
- K102556: Volpara, Version 1.3 (2010), 24 descendants of its own

## Indications for use
The Sectra IDS5 device is intended for the manipulation and displaying of medical images, including mammograms. It can show images from different modalities and interfaces to various image storage and printing devices using DICOM or similar interface standards. Device options make possible mammography reading, telecommunications; fast demonstration; prosthesis CAD; 3-D and angiography, etc.; and teleconferencing. Lossy compressed mammographic images are not intended for diagnostic review. Mammographic images should only be viewed with a monitor approved by FDA for viewing mammographic images. Typical users of this system are trained professionals, including but not limited to physicians, radiologists, nurses, medical technicians, and assistants.

Source page: https://510kreport.com/device/K050196
Methodology: https://510kreport.com/methodology