# K242051: VersaD Delivery Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Unity Medical, Inc.
- Decided: Jan 17, 2025 after 189 days
- Product code: QJP (Catheter, Percutaneous, Neurovasculature)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K010954 (2001). 15 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K200121: Route 92 Medical 088 Access System, 110 cm, Route 92 Medical, Inc. (2020) Summary page 5.

## Most influential descendants
- K251372: VersaD Delivery Catheter (2025), 0 descendants of its own

## Indications for use
The VersaD Delivery Catheter is intended for use with compatible guide catheters in facilitating the insertion and guidance of catheters into selected blood vessels in the neuro and peripheral vascular systems.

Source page: https://510kreport.com/device/K242051
Methodology: https://510kreport.com/methodology