# K073474: Capiox Circuit Connectors

- Pathway: 510(k) (Traditional)
- Applicant: Terumo Corp.
- Decided: Mar 5, 2008 after 85 days
- Product code: DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K895753 (1989). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041697: Terumo Circuit Connectors, Terumo Cardiovascular Systems Corporation (2004) Summary page 2.

## Indications for use
The Capiox Circuit Connectors are intended to be used to interconnect tubing and other devices in an extra-corporeal circuit during cardiopulmonary bypass procedures. The devices can be used in procedures lasting tup to 6 hours in duration.

Source page: https://510kreport.com/device/K073474
Methodology: https://510kreport.com/methodology