Nerivio; NerivioInfinity
K-Number: K241756 · 2024-10-08
ApplicantTheranica Bio-Electronics, Ltd.
Decision Date2024-10-08
Product CodeQGT
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Nerivio; NerivioInfinity is a medical device manufactured by Theranica Bio-Electronics, Ltd.. It received FDA 510(k) clearance on 2024-10-08 under approval number K241756. 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; NerivioInfinity?
Nerivio; NerivioInfinity is a medical device that received FDA 510(k) clearance on 2024-10-08. It is manufactured by Theranica Bio-Electronics, Ltd.. The 510(k) number is K241756.
When was Nerivio; NerivioInfinity approved by the FDA?
Nerivio; NerivioInfinity received FDA 510(k) clearance on 2024-10-08, under approval number K241756.
What company makes Nerivio; NerivioInfinity?
Nerivio; NerivioInfinity is manufactured by Theranica Bio-Electronics, Ltd..
What is the FDA product code for Nerivio; NerivioInfinity?
The FDA product code for Nerivio; NerivioInfinity 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.