Velano Vascular Q2 Extension Set
K-Number: K182897 · 2019-03-26
ApplicantVelano Vascular
Decision Date2019-03-26
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Velano Vascular Q2 Extension Set is a medical device manufactured by Velano Vascular. It received FDA 510(k) clearance on 2019-03-26 under approval number K182897. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Velano Vascular Q2 Extension Set?
Velano Vascular Q2 Extension Set is a medical device that received FDA 510(k) clearance on 2019-03-26. It is manufactured by Velano Vascular. The 510(k) number is K182897.
When was Velano Vascular Q2 Extension Set approved by the FDA?
Velano Vascular Q2 Extension Set received FDA 510(k) clearance on 2019-03-26, under approval number K182897.
What company makes Velano Vascular Q2 Extension Set?
Velano Vascular Q2 Extension Set is manufactured by Velano Vascular.
What is the FDA product code for Velano Vascular Q2 Extension Set?
The FDA product code for Velano Vascular Q2 Extension Set is FPA.
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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.