# Philips Digital Mammography Sweden AB

- Location (FDA's records): Solna, SE
- FDA decisions: 3 (2012–2013): 3 510(k) clearances
- Product codes: MUE (3)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Sectra-Imtec AB: 2 (https://510kreport.com/company/sectra-imtec)
- Matakina Technology Limited: 1 (https://510kreport.com/company/matakina-technology)
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)

## Its most-cited devices
- K123995: Microdose SI (2013), cited by 1
- K120255: Philips Microdose (2012), cited by 1

## Recent decisions
- K130704: Microdose SI (Dec 13, 2013)
- K123995: Microdose SI (Feb 1, 2013)
- K120255: Philips Microdose (Apr 19, 2012)

Source page: https://510kreport.com/company/philips-digital-mammography-sweden