Vibrant System
K-Number: K223031 · 2023-01-13
ApplicantVibrant, Ltd.
Decision Date2023-01-13
Product CodeQTN
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Vibrant System is a medical device manufactured by Vibrant, Ltd.. It received FDA 510(k) clearance on 2023-01-13 under approval number K223031. The device is classified under product code QTN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vibrant System?
Vibrant System is a medical device that received FDA 510(k) clearance on 2023-01-13. It is manufactured by Vibrant, Ltd.. The 510(k) number is K223031.
When was Vibrant System approved by the FDA?
Vibrant System received FDA 510(k) clearance on 2023-01-13, under approval number K223031.
What company makes Vibrant System?
Vibrant System is manufactured by Vibrant, Ltd..
What is the FDA product code for Vibrant System?
The FDA product code for Vibrant System is QTN.
Other Devices by Vibrant, Ltd.
Related Devices (Code: QTN)
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.