# K021893: G-Mops, Model 10030

- 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.
4 later devices descend from it; 2 cite 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. The FDA summary names its predicate without a number.
- (no number) ASP-100: named in the summary without a submission number
- (no number) Gamete-20/-100: named in the summary without a submission number

## Most influential descendants
- K081115: G-Mops G5 Series (2008), 2 descendants of its own
- K202862: Gx-IVF, Gx-TL, Gx-MOPS PLUS (2021), 0 descendants of its own
- K121128: Multipurpose Handling Medium (2012), 0 descendants of its own
- K032877: G-Oocyte (2004), 0 descendants of its own

## Indications for use
Medium for handling and manipulating oocytes and embryos in ambient atmosphere.

Source page: https://510kreport.com/device/K021893
Methodology: https://510kreport.com/methodology