# K982174: Venturi Ventilator

- Pathway: 510(k) (Traditional)
- Applicant: Cardiopulmonary Corp.
- Decided: Jun 24, 1998 after 7 days
- Product code: CBK (Ventilator, Continuous, Facility Use)
- Device class: 2
- Regulation: 21 CFR 868.5895
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The Venturi Ventilator is intended to mechanically control and assist the breathing of adult and pediatric patients. The Venturi is designed for hospital use under the direct supervision of a physician.

Source page: https://510kreport.com/device/K982174
Methodology: https://510kreport.com/methodology