# K902694: Coaxial Catheter Set

- Pathway: 510(k) (Traditional)
- Applicant: Cook Ob/Gyn
- Decided: Aug 28, 1990 after 70 days
- Product code: HDR (Cap, Cervical)
- Device class: 2
- Regulation: 21 CFR 884.5250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K172321: Shepard, Insemi-Cath, and Soft-Pass Coaxial - Cook Intrauterine Insemination Catheters (2017), 2 descendants of its own
- K231645: PherDal® At-Home Insemination Kit (2023), 0 descendants of its own
- K231203: Mosie Baby Kit (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K902694
Methodology: https://510kreport.com/methodology