# Janus Biomedical, Inc.

- Location (FDA's records): Austin, TX
- FDA decisions: 2 (1994–1996): 2 510(k) clearances
- Product codes: DTQ (1), LPZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Origen Biomedical, Inc.: 1 (https://510kreport.com/company/origen-biomedical)
- Jostra Bentley: 1 (https://510kreport.com/company/jostra-bentley)
- Maquet Cardiopulmonary, AG: 1 (https://510kreport.com/company/maquet-cardiopulmonary)

## Its most-cited devices
- K943803: Jostra HL-20 Integrated Perfusion System (1996), cited by 2
- K915471: Cryobag (1994), cited by 1

## Recent decisions
- K943803: Jostra HL-20 Integrated Perfusion System (Jan 30, 1996)
- K915471: Cryobag (Mar 2, 1994)

Source page: https://510kreport.com/company/janus-biomedical