Vitesse (5.0)
K-Number: K241876 · 2024-10-23
ApplicantVarian Medical Systems
Decision Date2024-10-23
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Vitesse (5.0) is a medical device manufactured by Varian Medical Systems. It received FDA 510(k) clearance on 2024-10-23 under approval number K241876. 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 Vitesse (5.0)?
Vitesse (5.0) is a medical device that received FDA 510(k) clearance on 2024-10-23. It is manufactured by Varian Medical Systems. The 510(k) number is K241876.
When was Vitesse (5.0) approved by the FDA?
Vitesse (5.0) received FDA 510(k) clearance on 2024-10-23, under approval number K241876.
What company makes Vitesse (5.0)?
Vitesse (5.0) is manufactured by Varian Medical Systems.
What is the FDA product code for Vitesse (5.0)?
The FDA product code for Vitesse (5.0) 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.