# K021890: G-2 Version 3, Model 10049

- Pathway: 510(k) (Traditional)
- Applicant: Vitrolife Sweden AB
- Decided: Sep 6, 2002 after 88 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) G2.2TM: named in the summary without a submission number

## Most influential descendants
- K081117: G-2 V5 (2008), 0 descendants of its own

## Indications for use
Medium for culture of embryos from day 3 to the blastocyst stage.

Source page: https://510kreport.com/device/K021890
Methodology: https://510kreport.com/methodology