# K830728: Cardiovascular Disposable Products

- Pathway: 510(k) (Traditional)
- Applicant: Electromics, Inc.
- Decided: Apr 28, 1983 after 51 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K992906: Components for Cardiovascular Procedure Kit (1999), 1 descendant of its own
- K093992: Terumo Lauer Lock Adapter (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K830728
Methodology: https://510kreport.com/methodology