LVivo IQS
K-Number: K222970 · 2023-02-01
ApplicantDia Imaging Analysis, Ltd.
Decision Date2023-02-01
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
LVivo IQS is a medical device manufactured by Dia Imaging Analysis, Ltd.. It received FDA 510(k) clearance on 2023-02-01 under approval number K222970. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LVivo IQS?
LVivo IQS is a medical device that received FDA 510(k) clearance on 2023-02-01. It is manufactured by Dia Imaging Analysis, Ltd.. The 510(k) number is K222970.
When was LVivo IQS approved by the FDA?
LVivo IQS received FDA 510(k) clearance on 2023-02-01, under approval number K222970.
What company makes LVivo IQS?
LVivo IQS is manufactured by Dia Imaging Analysis, Ltd..
What is the FDA product code for LVivo IQS?
The FDA product code for LVivo IQS is QIH.
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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.