# K992906: Components for Cardiovascular Procedure Kit

- Pathway: 510(k) (Traditional)
- Applicant: Olson Medical Sales, Inc.
- Decided: Nov 10, 1999 after 72 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: 1 generation back to K790563 (1979). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K790563: Adapters-Y-Type, Dlp, Inc. (1979) Summary page 1.
- K830728: Cardiovascular Disposable Products, Electromics, Inc. (1983) Summary page 1.

## Most influential descendants
- K093992: Terumo Lauer Lock Adapter (2010), 0 descendants of its own

## Indications for use
The Adapters are intended to be used to interconnect tubing and other devices during cardiopulmonary bypass procedures.

Source page: https://510kreport.com/device/K992906
Methodology: https://510kreport.com/methodology