# Vitrolife AB/Scandinavian Ivf Sciences AB

- Location (FDA's records): Washington, DC
- FDA decisions: 7 (2000–2000): 7 510(k) clearances
- Product codes: MQL (7)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Medicult A/S: 2 (https://510kreport.com/company/medicult-a-s)
- Nidacon International AB: 1 (https://510kreport.com/company/nidacon-international)

## Its most-cited devices
- K000625: Scandinavian Ivf Sciences AB, G1.2 (2000), cited by 1
- K000621: Scandinavian Ivf Sciences AB, Spermrinse -20/100 (2000), cited by 1
- K000619: Scandinavian Ivf Sciences AB, G2.2 (2000), cited by 1

## Recent decisions
- K000619: Scandinavian Ivf Sciences AB, G2.2 (Jun 27, 2000)
- K000627: Scandinavian Ivf Sciences AB, Hybase-1 (Jun 13, 2000)
- K000625: Scandinavian Ivf Sciences AB, G1.2 (May 23, 2000)
- K000626: Scandinavian Ivf Sciences AB, Gamete-100 (May 23, 2000)
- K000618: Scandinavian Ivf Sciences AB, Thaw-Kit 1 (May 17, 2000)
- K000623: Scandinavian Ivf Sciences AB, Freeze-Kit 1 (May 16, 2000)
- K000621: Scandinavian Ivf Sciences AB, Spermrinse -20/100 (May 16, 2000)

Source page: https://510kreport.com/company/vitrolife-ab-scandinavian-ivf-sciences