# K240375: V80 Anesthetic Vaporizer (V80)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
- Decided: Oct 31, 2024 after 267 days
- Product code: CAD (Vaporizer, Anesthesia, Non-Heated)
- Device class: 2
- Regulation: 21 CFR 868.5880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K940255 (1994). 4 ancestors in all.
No later device cites it as a predicate yet.
1 of 5 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042276: D-Vapor, Draeger Medical, Inc. (2004) Summary page 5.

## Indications for use
V80 Anesthetic Vaporizer is used to enrich the fresh gas flow of an anesthesia delivery system with controllable desflurane vapour. V80 Anesthetic Vaporizer is intended to be operated only by licensed clinicians and qualified anesthesia personnel who have received adequate training in its use. Anyone unauthorized or untrained must not perform any operation on the anesthetic vaporizer. V80 Anesthetic Vaporizer cannot be used in mobile vehicles, airplanes, helicopters or ships. V80 Anesthetic Vaporizer is not suitable for use in an MRI environment.

Source page: https://510kreport.com/device/K240375
Methodology: https://510kreport.com/methodology