# K930620: Bard (R) William Harvey (R) Arterial Straigh Cannula

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: May 7, 1993 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: 2 (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
- K063618: Tenderflow Periatric Arterial Cannula (2007), 0 descendants of its own

## Recalls of this device
- Dec 7, 2006 · Not classified · Z-0544-2007: The cannula connector is an incorrect size: It is actually 1/4" by 3/8" instead of the correct 1/4" by 1/4".
- Dec 7, 2006 · Not classified · Z-0543-2007: The cannula connector is an incorrect size: It is actually 1/4" by 3/8" instead of the correct 1/4" by 1/4".

Source page: https://510kreport.com/device/K930620
Methodology: https://510kreport.com/methodology