# Scanditronix, Inc.

- Location (FDA's records): Sweden, SE
- FDA decisions: 7 (1984–1994): 7 510(k) clearances
- Product codes: IYE (3), IWE (1), KPS (1), IWB (1), KPQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Scanditronix Medical AB: 4 (https://510kreport.com/company/scanditronix-medical)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)

## Its most-cited devices
- K934303: RFA A-300 (1994), cited by 2
- K925133: DPD-510 Therapeutic Radiation Dosimeter (1993), cited by 1
- K942092: DPD-3 (1994), cited by 1
- K914926: Scandiplan - Version 338 (1992), cited by 1

## Recent decisions
- K934303: RFA A-300 (Aug 9, 1994)
- K942092: DPD-3 (Jul 29, 1994)
- K925133: DPD-510 Therapeutic Radiation Dosimeter (Jan 4, 1993)
- K914926: Scandiplan - Version 338 (May 28, 1992)
- K904753: Diolase (Nov 9, 1990)
- K900434: MM-22 Microtron, MM50 Microtron (Oct 23, 1990)
- K843366: Superpett (Nov 21, 1984)

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