# K023622: Stockert Pediatric Aortic Cannulae, Model Numbers A272-15 Through A272-35

- Pathway: 510(k) (Abbreviated)
- Applicant: Stockert Instrumente GmbH
- Decided: Nov 21, 2002 after 23 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) Jostra Arterial Perfusion Cannulae: named in the summary without a submission number
- (no number) Research Medical Inc. Pediatric Aortic Cannula: named in the summary without a submission number

## Indications for use
The Stockert Pediatric Aortic Cannulae are designed to be used as perfusion cannulae to return arterial blood from the extracorporeal circuit to the patient during cardiopulmonary bypass up to six hours or less.

Source page: https://510kreport.com/device/K023622
Methodology: https://510kreport.com/methodology