Nerivio
K-Number: K201824 · 2020-10-23
ApplicantTheranica Bio-Electronics, Ltd.
Decision Date2020-10-23
Product CodeQGT
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Nerivio is a medical device manufactured by Theranica Bio-Electronics, Ltd.. It received FDA 510(k) clearance on 2020-10-23 under approval number K201824. The device is classified under product code QGT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nerivio?
Nerivio is a medical device that received FDA 510(k) clearance on 2020-10-23. It is manufactured by Theranica Bio-Electronics, Ltd.. The 510(k) number is K201824.
When was Nerivio approved by the FDA?
Nerivio received FDA 510(k) clearance on 2020-10-23, under approval number K201824.
What company makes Nerivio?
Nerivio is manufactured by Theranica Bio-Electronics, Ltd..
What is the FDA product code for Nerivio?
The FDA product code for Nerivio is QGT.
Other Devices by Theranica Bio-Electronics, Ltd.
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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.