Radiance V4
K-Number: K171885 · 2017-07-25
Decision Date2017-07-25
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Radiance V4 is a medical device manufactured by Gmv Soluciones Globales Internet S.A.U.. It received FDA 510(k) clearance on 2017-07-25 under approval number K171885. 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 V4?
Radiance V4 is a medical device that received FDA 510(k) clearance on 2017-07-25. It is manufactured by Gmv Soluciones Globales Internet S.A.U.. The 510(k) number is K171885.
When was Radiance V4 approved by the FDA?
Radiance V4 received FDA 510(k) clearance on 2017-07-25, under approval number K171885.
What company makes Radiance V4?
Radiance V4 is manufactured by Gmv Soluciones Globales Internet S.A.U..
What is the FDA product code for Radiance V4?
The FDA product code for Radiance V4 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.