# K022321: Stockert V172-28 Venous Femoral Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Stockert Instrumente GmbH
- Decided: Oct 9, 2002 after 84 days
- Product code: DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Medtronic DLP Venous Femoral Cannula: named in the summary without a submission number

## Indications for use
The Stockert V 172-28 Venous Femoral Cannula is intended to be used to cannulate the inferior vena cava and the right atrium via femoral access during cardiopulmonary bypass surgery for periods up to six hours.

Source page: https://510kreport.com/device/K022321
Methodology: https://510kreport.com/methodology