# K023379: Coopersurgical Embryo Transfer Catheter, Coopersurgical Assisted Reproduction Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cooper Surgical
- Decided: Dec 11, 2002 after 64 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
Longest line of descent: 1 generation back to K990350 (1999). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K990350: Wallace Catheters-18CM, Model 1816; 23CM, Model 1816N; 23CM, Model 2316, CooperSurgical, Inc. (1999) Summary page 1.

## Most influential descendants
- K053208: Clear Vision Embryo Transfer Catheter Set, Model B100000 - B 100007; Clear Vision Trial Transfer Catheter Set (2006), 0 descendants of its own

## Indications for use
The sterile single-use device is to be used for the introduction of embryo(s) into the uterine cavity during assisted reproductive procedures.

Source page: https://510kreport.com/device/K023379
Methodology: https://510kreport.com/methodology