Vyvo
K-Number: K231288 · 2024-03-04
ApplicantVyvo Technology Corp.(Vt)
Decision Date2024-03-04
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Vyvo is a medical device manufactured by Vyvo Technology Corp.(Vt). It received FDA 510(k) clearance on 2024-03-04 under approval number K231288. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vyvo?
Vyvo is a medical device that received FDA 510(k) clearance on 2024-03-04. It is manufactured by Vyvo Technology Corp.(Vt). The 510(k) number is K231288.
When was Vyvo approved by the FDA?
Vyvo received FDA 510(k) clearance on 2024-03-04, under approval number K231288.
What company makes Vyvo?
Vyvo is manufactured by Vyvo Technology Corp.(Vt).
What is the FDA product code for Vyvo?
The FDA product code for Vyvo is DQA.
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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.