# Althin Medical AB

- Location (FDA's records): Ronneby, SE
- FDA decisions: 7 (1999–2000): 7 510(k) clearances
- Product codes: KDI (4), FJI (2), KPO (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 1 (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
- Althin Medical AB an Affiliate of Baxter Intl: 6 (https://510kreport.com/company/althin-medical-ab-an-affiliate-of-baxter-intl)
- Gambro, Inc.: 1 (https://510kreport.com/company/gambro)
- C.G.H. Medical, Inc.: 1 (https://510kreport.com/company/cgh-medical)

## Firms that cite its devices most
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)

## Its most-cited devices
- K992573: AF-220 Hemodialyzer (2000), cited by 1

## Recent decisions
- K992563: A-22 Hemodialyzer (Jan 18, 2000)
- K992564: AF-180 Hemodialyzer (Jan 18, 2000)
- K992573: AF-220 Hemodialyzer (Jan 18, 2000)
- K992566: AF-150 Hemodialyzer (Jan 18, 2000)
- K992594: A-15 Hemodialyzer (Sep 24, 1999)
- K992565: A-18 Hemodialyzer (Sep 23, 1999)
- K990010: Althin Medical AB Altracart II (Apr 15, 1999)

Source page: https://510kreport.com/company/althin-medical