LVivo Seamless
K-Number: K243331 · 2025-03-06
ApplicantDia Imaging Analysis, Ltd.
Decision Date2025-03-06
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
LVivo Seamless is a medical device manufactured by Dia Imaging Analysis, Ltd.. It received FDA 510(k) clearance on 2025-03-06 under approval number K243331. 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 Seamless?
LVivo Seamless is a medical device that received FDA 510(k) clearance on 2025-03-06. It is manufactured by Dia Imaging Analysis, Ltd.. The 510(k) number is K243331.
When was LVivo Seamless approved by the FDA?
LVivo Seamless received FDA 510(k) clearance on 2025-03-06, under approval number K243331.
What company makes LVivo Seamless?
LVivo Seamless is manufactured by Dia Imaging Analysis, Ltd..
What is the FDA product code for LVivo Seamless?
The FDA product code for LVivo Seamless 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.