V80 Anesthetic Vaporizer (V80)
K-Number: K240375 · 2024-10-31
Decision Date2024-10-31
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
V80 Anesthetic Vaporizer (V80) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2024-10-31 under approval number K240375. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the V80 Anesthetic Vaporizer (V80)?
V80 Anesthetic Vaporizer (V80) is a medical device that received FDA 510(k) clearance on 2024-10-31. It is manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K240375.
When was V80 Anesthetic Vaporizer (V80) approved by the FDA?
V80 Anesthetic Vaporizer (V80) received FDA 510(k) clearance on 2024-10-31, under approval number K240375.
What company makes V80 Anesthetic Vaporizer (V80)?
V80 Anesthetic Vaporizer (V80) is manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd..
What is the FDA product code for V80 Anesthetic Vaporizer (V80)?
The FDA product code for V80 Anesthetic Vaporizer (V80) is CAD.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.