# K251372: VersaD Delivery Catheter

- Pathway: 510(k) (Special)
- Applicant: Unity Medical, Inc.
- Decided: Oct 24, 2025 after 175 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: 9 generations back to K010954 (2001). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K242051: VersaD Delivery Catheter, Unity Medical, Inc. (2025) Summary page 5.

## 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/K251372
Methodology: https://510kreport.com/methodology