# B. Braun Medizintechnologie GmbH

- Location (FDA's records): Melsungen, DE
- FDA decisions: 3 (2006–2008): 3 510(k) clearances
- Product codes: KDI (1), FKQ (1), KPO (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 5 (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
- Gambro Renal Products: 2 (https://510kreport.com/company/gambro-renal-products)
- Clarigen, Inc.: 1 (https://510kreport.com/company/clarigen)
- Minntech Corp.: 1 (https://510kreport.com/company/minntech)

## Firms that cite its devices most
- B. Braun Avitum AG: 4 (https://510kreport.com/company/b-braun-avitum)
- Di-Chem, Inc.: 1 (https://510kreport.com/company/di-chem)

## Its most-cited devices
- K071518: Diacap LO PS (10, 12, 15) and Diacap HI PS (10, 12, 15, 18, 20) Hemodialyzers (2007), cited by 3
- K072760: Solcart B (2008), cited by 2

## Recent decisions
- K072760: Solcart B (Jan 29, 2008)
- K071518: Diacap LO PS (10, 12, 15) and Diacap HI PS (10, 12, 15, 18, 20) Hemodialyzers (Aug 17, 2007)
- K052764: Diacap Ultra Dialysis Fluid Filter (Jun 9, 2006)

Source page: https://510kreport.com/company/b-braun-medizintechnologie