# K993062: Chest Drainage Tubing

- Pathway: 510(k) (Traditional)
- Applicant: Olson Medical Sales, Inc.
- Decided: Dec 10, 1999 after 88 days
- Product code: DWE (Tubing, Pump, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4390
- 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 K870792 (1987). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K870792: Thorastat Atr-XXXX, Gish Biomedical, Inc. (1987) Summary page 1.

## Indications for use
The Chest Drainage Tubing is intended to serve as a conduit for the flow of body fluids that are removed from the patient, via vacuum, and delivered to a reservoir during cardiopulmonary bypass procedures

Source page: https://510kreport.com/device/K993062
Methodology: https://510kreport.com/methodology