# K010906: Medtronic Stylet Kit, Models 6282, 6293, and 6254

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Vascular
- Decided: Apr 5, 2001 after 10 days
- Product code: DRB (Stylet, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1380
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
1 of 3 devices in its family (counting itself) has 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
- K063210: Attain Hybrid Guide Wires, Model GWR419378, GWR419388, GWR419478, GWR419488 (2007), 1 descendant of its own
- K143316: Attain Hybrid Guide Wire (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K010906
Methodology: https://510kreport.com/methodology