# K233791: Drivewire 24 Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Rapid-Medical, Ltd.
- Decided: Jul 11, 2024 after 226 days
- Product code: MOF (Guide, Wire, Catheter, Neurovasculature)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K002212 (2000). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192783: Aristotle 24 Guidewire, 200cm, Soft Profile ; Aristotle 24 Guidewire, 200cm, Standard Profile ; Aristotle 24 Guidewire, 200cm, Support Profile, Scientia Vascular, LLC (2019) Summary page 4.

## Most influential descendants
- K254006: Drivewire 35 Guidewire (2026), 0 descendants of its own

## Indications for use
The Drivewire 24 Guidewire is intended for general intravascular use, including the neuro and peripheral vasculature. The Drivewire 24 Guidewire is intended to facilitate the selective placement of diagnostic or therapeutic catheters. This device is not intended for use in the coronary arteries.

Source page: https://510kreport.com/device/K233791
Methodology: https://510kreport.com/methodology