VEA Align
K-Number: K231917 · 2024-01-05
ApplicantEos Imaging
Decision Date2024-01-05
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
VEA Align is a medical device manufactured by Eos Imaging. It received FDA 510(k) clearance on 2024-01-05 under approval number K231917. 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 VEA Align?
VEA Align is a medical device that received FDA 510(k) clearance on 2024-01-05. It is manufactured by Eos Imaging. The 510(k) number is K231917.
When was VEA Align approved by the FDA?
VEA Align received FDA 510(k) clearance on 2024-01-05, under approval number K231917.
What company makes VEA Align?
VEA Align is manufactured by Eos Imaging.
What is the FDA product code for VEA Align?
The FDA product code for VEA Align 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.