# K022280: Stockert Coronary Perfusion Cannulae

- Pathway: 510(k) (Abbreviated)
- Applicant: Stockert Instrumente GmbH
- Decided: Oct 11, 2002 after 88 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 Coronary Ostial Perfusion Cannulae: named in the summary without a submission number

## Indications for use
The Stockert Coronary Perfusion Cannulae are intended to be used to cannulate the coronary ostium and to deliver cardioplegic solution during cardiopulmonary surgery for periods of up to six hours.

Source page: https://510kreport.com/device/K022280
Methodology: https://510kreport.com/methodology