# K000625: Scandinavian Ivf Sciences AB, G1.2

- Pathway: 510(k) (Traditional)
- Applicant: Vitrolife AB/Scandinavian Ivf Sciences AB
- Decided: May 23, 2000 after 96 days
- Product code: MQL (Media, Reproductive)
- Device class: 2
- Regulation: 21 CFR 884.6180
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K030490: ISM1+, IMS2+, and Utm+ (2003), 3 descendants of its own
- K080473: Embryoassist and Embryoassist with Phenol Red (2008), 2 descendants of its own
- K120136: Embryogen (2012), 1 descendant of its own
- K140317: Embryogen (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K000625
Methodology: https://510kreport.com/methodology
