# Apriomed AB

- Location (FDA's records): Uppsala, SE
- FDA decisions: 3 (2015–2020): 3 510(k) clearances
- Product codes: KNW (2), FCG (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Bard Gynecology and Radiology: 1 (https://510kreport.com/company/bard-gynecology-and-radiology)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Medical Device Technologies, Inc.: 1 (https://510kreport.com/company/medical-device-technologies)
- Gallini Intl., Inc.: 1 (https://510kreport.com/company/gallini-intl)

## Recent decisions
- K193268: APrioCore Plus (Feb 27, 2020)
- K181756: Gangi-SoftGuard Coaxial Needle, Gangi-HydroGuard Coaxial Needle (Dec 18, 2018)
- K150625: Morrison Steerable Needle (Jun 9, 2015)

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