LVivo IQS
K-Number: K240769 · 2024-05-24
ApplicantDia Imaging Analysis, Ltd.
Decision Date2024-05-24
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 2024-05-24 under approval number K240769. 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 2024-05-24. It is manufactured by Dia Imaging Analysis, Ltd.. The 510(k) number is K240769.
When was LVivo IQS approved by the FDA?
LVivo IQS received FDA 510(k) clearance on 2024-05-24, under approval number K240769.
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.