# Fresenius Hemotechnology, Inc.

- Location (FDA's records): Concord, CA
- FDA decisions: 3 (1999–2001): 3 510(k) clearances
- Product codes: CAC (2), DTN (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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
- Haemonetics Corp.: 1 (https://510kreport.com/company/haemonetics)
- Electromedics, Inc.: 1 (https://510kreport.com/company/electromedics)
- Shiley, Inc.: 1 (https://510kreport.com/company/shiley)

## Recent decisions
- K012178: Fresenius C.a.T.S; Ati Autotransfusion Set; PSQ Plasma Sequestration Set; PSQ-DD Plasma Sequestration Direct Draw (Jul 23, 2001)
- K984586: Fresenius ATR40 and ATR120 Autotransfusion Reservoirs (Jun 29, 1999)
- K984233: C.a.T.S Autotransfusion Accessories, Models Ats Suction Line, Aty Y-Adapter, and Ato Oxygenator Line (Feb 1, 1999)

Source page: https://510kreport.com/company/fresenius-hemotechnology