BeneVision Central Monitoring System
K-Number: K193391 · 2020-05-21
Decision Date2020-05-21
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
BeneVision Central Monitoring System is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2020-05-21 under approval number K193391. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BeneVision Central Monitoring System?
BeneVision Central Monitoring System is a medical device that received FDA 510(k) clearance on 2020-05-21. It is manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K193391.
When was BeneVision Central Monitoring System approved by the FDA?
BeneVision Central Monitoring System received FDA 510(k) clearance on 2020-05-21, under approval number K193391.
What company makes BeneVision Central Monitoring System?
BeneVision Central Monitoring System is manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd..
What is the FDA product code for BeneVision Central Monitoring System?
The FDA product code for BeneVision Central Monitoring System is MSX.
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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.