Velocity
K-Number: K173636 · 2018-02-15
ApplicantVarian Medical Systems, Inc.
Decision Date2018-02-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Velocity is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2018-02-15 under approval number K173636. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Velocity?
Velocity is a medical device that received FDA 510(k) clearance on 2018-02-15. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K173636.
When was Velocity approved by the FDA?
Velocity received FDA 510(k) clearance on 2018-02-15, under approval number K173636.
What company makes Velocity?
Velocity is manufactured by Varian Medical Systems, Inc..
What is the FDA product code for Velocity?
The FDA product code for Velocity is LLZ.
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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.