# Jostra Medizintechnik AG

- Location (FDA's records): Newark, DE
- FDA decisions: 2 (2000–2000): 2 510(k) clearances
- Product codes: KFM (1), DTM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Maquet Cardiopulmonary, AG: 4 (https://510kreport.com/company/maquet-cardiopulmonary)
- Stockert Instrumente GmbH: 2 (https://510kreport.com/company/stockert-instrumente)
- Inspira Technologies Oxy B.H.N., Ltd.: 1 (https://510kreport.com/company/inspira-technologies-oxy-bhn)
- Abiomed, Inc.: 1 (https://510kreport.com/company/abiomed)
- Fresenius Medical Care Renal Therapies Group, LLC: 1 (https://510kreport.com/company/fresenius-medical-care-renal-therapies-group)
- Cardiovention, Inc.: 1 (https://510kreport.com/company/cardiovention)
- International Biophysics Corp.: 1 (https://510kreport.com/company/international-biophysics)

## Its most-cited devices
- K991864: Rotaflow Centrifugal Pump System (2000), cited by 9
- K001787: Quart Arterial Filter, Model HBF 140 (2000), cited by 2

## Recent decisions
- K991864: Rotaflow Centrifugal Pump System (Aug 31, 2000)
- K001787: Quart Arterial Filter, Model HBF 140 (Jun 30, 2000)

Source page: https://510kreport.com/company/jostra-medizintechnik