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FDA 510(k)

Nerivio

K-Number: K223169 · 2023-02-06

ApplicantTheranica Bioelectronics , Ltd.
Decision Date2023-02-06
Product CodeQGT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Nerivio is a medical device manufactured by Theranica Bioelectronics , Ltd.. It received FDA 510(k) clearance on 2023-02-06 under approval number K223169. 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 2023-02-06. It is manufactured by Theranica Bioelectronics , Ltd.. The 510(k) number is K223169.

When was Nerivio approved by the FDA?

Nerivio received FDA 510(k) clearance on 2023-02-06, under approval number K223169.

What company makes Nerivio?

Nerivio is manufactured by Theranica Bioelectronics , Ltd..

What is the FDA product code for Nerivio?

The FDA product code for Nerivio is QGT.

Other Devices by Theranica Bioelectronics , Ltd.

DEN180059Nerivio Migra K203181Nerivio, FGD000075-4.7 K232152NerivioInfinity

Related Devices (Code: QGT)

DEN180059Nerivio MigraTheranica Bioelectronics , Ltd. K201824NerivioTheranica Bio-Electronics, Ltd. K203181Nerivio, FGD000075-4.7Theranica Bioelectronics , Ltd. K232152NerivioInfinityTheranica Bioelectronics , Ltd. K241756Nerivio; NerivioInfinityTheranica Bio-Electronics, Ltd. K250405Nerivio; Nerivio InfinityTheranica Bio-Electronics, Ltd.

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.

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