# K020983: Jostra Suckers, Model JS

- Pathway: 510(k) (Traditional)
- Applicant: Jostra AG
- Decided: Jan 30, 2004 after 674 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 Suction Devices: named in the summary without a submission number

## Indications for use
The Jostra Suction Devices are designed to aspirate blood and other fluids from the operative field and return it to the extracorporeal circuit during open heart surgery lasting 6 hours or less.

Source page: https://510kreport.com/device/K020983
Methodology: https://510kreport.com/methodology