# K013963: Model 9210 Delivery Catheter, Model 9210

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Vascular
- Decided: Feb 28, 2002 after 87 days
- Product code: DQY (Catheter, Percutaneous)
- 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: 1 generation back to K950179 (1995). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K950179: Medtronic (R) GC Iii Coronary Guiding Catheter, Medtronics Interventional Vascular (1995) Summary page 2.

## Most influential descendants
- K022620: Sheathless Accessory Kit, Models XRIK24, XRIK28, XRIK32, XRIK36, XRIK40 and Xrikrt (2002), 0 descendants of its own

## Indications for use
The Medtronic Model 9210 Delivery Catheter is intended for device passage and placement within the venous vessels and chambers of the heart.

Source page: https://510kreport.com/device/K013963
Methodology: https://510kreport.com/methodology