NEURALIEVE CERENA TRANSCRANIAL MAGNETIC STIMULATOR— 510(k) DEN130022

Name: FDA 510(k) clearance DEN130022
Creator: U.S. Food and Drug Administration
Published: 2013-12-13

Unknown

Eneura Therapeutics

FDA 510(k) clearance DEN130022 for NEURALIEVE CERENA TRANSCRANIAL MAGNETIC STIMULATOR, Unknown on 2013-12-13. Applicant: Eneura Therapeutics. Device class: 2.

Clearance details

Applicant: Eneura Therapeutics
Product code: Code OKP
Device class: Class 2
Regulation: 21 CFR 882.5808
Advisory panel: Neurology
Date received: 2013-03-05
Decision date: 2013-12-13
Decision: Unknown
Clearance type: Direct
Location: Orono, MN, US

View on FDA.gov ↗

Recent devices under product code OKP

view all

K230358 — SAVI Dual (TM) Migraine Therapy2023-05-16
K182976 — SpringTMS2019-02-25
K162797 — SpringTMS2017-06-26
K161663 — sTMS mini2016-08-23
K140094 — SPRINGTMS TOTAL MIGRAINE SYSTEM2014-05-21

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