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FDA 510(k)

HYPERVISOR VI CENTRAL MONITORING SYSTEM

K-Number: K062194 · 2007-04-11

ApplicantShenzhen Mindray Bio-Medical Electronics Co., Ltd.
Decision Date2007-04-11
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HYPERVISOR VI CENTRAL MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2007-04-11 under 510(k) number K062194. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPERVISOR VI CENTRAL MONITORING SYSTEM?

HYPERVISOR VI CENTRAL MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2007-04-11. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K062194.

When did HYPERVISOR VI CENTRAL MONITORING SYSTEM receive FDA 510(k) clearance?

HYPERVISOR VI CENTRAL MONITORING SYSTEM received FDA 510(k) clearance on 2007-04-11, under 510(k) number K062194.

Who is the listed applicant for HYPERVISOR VI CENTRAL MONITORING SYSTEM?

The FDA 510(k) record lists Shenzhen Mindray Bio-Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYPERVISOR VI CENTRAL MONITORING SYSTEM?

The FDA product code for HYPERVISOR VI CENTRAL MONITORING SYSTEM is MHX.

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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.

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