TIVA¿
K-Number: K152924 · 2016-01-07
ApplicantVelano Vascular
Decision Date2016-01-07
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent
Device Summary
TIVA¿ is a medical device manufactured by Velano Vascular. It received FDA 510(k) clearance on 2016-01-07 under approval number K152924. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TIVA¿?
TIVA¿ is a medical device that received FDA 510(k) clearance on 2016-01-07. It is manufactured by Velano Vascular. The 510(k) number is K152924.
When was TIVA¿ approved by the FDA?
TIVA¿ received FDA 510(k) clearance on 2016-01-07, under approval number K152924.
What company makes TIVA¿?
TIVA¿ is manufactured by Velano Vascular.
What is the FDA product code for TIVA¿?
The FDA product code for TIVA¿ is JKA.
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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.