# K854487: Venous Return Cannula W/Cuff 91039

- Pathway: 510(k) (Traditional)
- Applicant: Dlp, Inc.
- Decided: Feb 10, 1986 after 94 days
- Product code: DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4210
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K120987: DLP Single Stage Venous Cannula Inflatable Cuff (2012), 0 descendants of its own

## Recalls of this device
- Dec 14, 2011 · Not classified · Z-0811-2012: Instructions for Use for the DLP Single Stage Venous Cannulae are in the process of being updated. The current precaution statement referencing ventricular assist procedures will be identified as a co

Source page: https://510kreport.com/device/K854487
Methodology: https://510kreport.com/methodology