# K991266: <Genx> Embryo Transfer Catheter CC Glider

- Pathway: 510(k) (Traditional)
- Applicant: <Genx> Intl., Inc.
- Decided: Sep 9, 1999 after 149 days
- Product code: MQF (Catheter, Assisted Reproduction)
- Device class: 2
- Regulation: 21 CFR 884.6110
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
Embryo Transfer Catheter used to introduce embryos into the body.

Source page: https://510kreport.com/device/K991266
Methodology: https://510kreport.com/methodology