# K840001: Arterial Cannula Straight Beveled Tip

- Pathway: 510(k) (Traditional)
- Applicant: Dlp, Inc.
- Decided: Feb 13, 1984 after 41 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.
13 later devices descend from it; 2 cite it directly.
0 of 14 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
- K024069: One Piece Pediatric Arterial Cannula, Model: 77006, 77106 (2003), 6 descendants of its own
- K111972: Affinity CP Centrifugal Pump, Resting Heart Sys.,Myotherm Cardioplegia Deliv.,Affinity Hollow Fiber Oxygenator,Aaf (2011), 5 descendants of its own
- K120988: DLP Single Stage Venous Cannula, DLP Right Angle Single Stage Venous Cannula, DLP Single Stage Venous Cannula with Right (2012), 4 descendants of its own
- K143083: Bio-Medicus Pediatric Cannula and Introducers (2015), 3 descendants of its own
- K201100: Bio-Medicus Life Support Catheter and Introducer (2021), 2 descendants of its own

## Recalls of this device
- May 9, 2008 · Not classified · Z-1925-2008: Medtronic is recalling selected Carmeda-coated cardiopulmonary bypass (CPB) products (e.g., oxygenators, reservoirs, pumps, cannulae and tubing packs) that were manufactured with contaminated heparin.

Source page: https://510kreport.com/device/K840001
Methodology: https://510kreport.com/methodology