Nerivio Migra— 510(k) DEN180059

Unknown

Theranica Bioelectronics , Ltd.

FDA 510(k) clearance DEN180059 for Nerivio Migra, Unknown on 2019-05-20. Applicant: Theranica Bioelectronics , Ltd.. Device class: 2.

Clearance details

Applicant: Theranica Bioelectronics , Ltd.
Product code: Code QGT
Device class: Class 2
Regulation: 21 CFR 882.5899
Advisory panel: Neurology
Date received: 2018-11-06
Decision date: 2019-05-20
Decision: Unknown
Clearance type: Direct
Location: Netanya, IL

View on FDA.gov ↗

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K223169 — Nerivio2023-02-06
K203181 — Nerivio, FGD000075-4.72021-01-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.