# K132903: Dre Ventura

- Pathway: 510(k) (Traditional)
- Applicant: Dre Medical, Inc.
- Decided: Jul 1, 2014 after 288 days
- Product code: BSZ (Gas-Machine, Anesthesia)
- Device class: 2
- Regulation: 21 CFR 868.5160
- 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 K844008 (1985). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061102: Prima Anaesthesia Machine, Penlon, Ltd. (2006) Summary page 1.

## Indications for use
The Ventura anesthesia gas delivery machine is designed to deliver a combination of medical gases and volatile anesthetic agents to a breathing system.

Source page: https://510kreport.com/device/K132903
Methodology: https://510kreport.com/methodology