# Sectra AB

- Location (FDA's records): Linköping, SE
- FDA decisions: 5 (2000–2024): 5 510(k) clearances
- Product codes: LLZ (3), PSY (1), QKQ (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medis Medical Imaging Systems BV: 4 (https://510kreport.com/company/medis-medical-imaging-systems)
- Leica Biosystems Imaging, Inc.: 2 (https://510kreport.com/company/leica-biosystems-imaging)
- Sectra-Imtec AB: 1 (https://510kreport.com/company/sectra-imtec)

## Firms that cite its devices most
- Infinitt Co., Ltd.: 1 (https://510kreport.com/company/infinitt)
- Realtimeimage, Inc.: 1 (https://510kreport.com/company/realtimeimage)

## Its most-cited devices
- K034059: Sectra Angiography Package and Sectra Cardiology Package (2004), cited by 2

## Recent decisions
- K232208: Sectra Digital Pathology Module (Version 3.3) (Apr 16, 2024)
- K193054: Sectra Digital Pathology Module (Mar 31, 2020)
- K034059: Sectra Angiography Package and Sectra Cardiology Package (Mar 9, 2004)
- K033088: Sectra IDS5 Radiology Workstation Version 10.1 (Oct 29, 2003)
- K001140: IDS5 Image Display System (May 3, 2000)

Source page: https://510kreport.com/company/sectra