Radiance V5
K-Number: K233236 · 2024-05-17
Decision Date2024-05-17
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Radiance V5 is a medical device manufactured by Gmv Soluciones Globales Internet S.A.U.. It received FDA 510(k) clearance on 2024-05-17 under approval number K233236. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Radiance V5?
Radiance V5 is a medical device that received FDA 510(k) clearance on 2024-05-17. It is manufactured by Gmv Soluciones Globales Internet S.A.U.. The 510(k) number is K233236.
When was Radiance V5 approved by the FDA?
Radiance V5 received FDA 510(k) clearance on 2024-05-17, under approval number K233236.
What company makes Radiance V5?
Radiance V5 is manufactured by Gmv Soluciones Globales Internet S.A.U..
What is the FDA product code for Radiance V5?
The FDA product code for Radiance V5 is MUJ.
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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.