FDA 510(k) Applications for Medical Device Product Code "OKP"

FDA 510(k) Number Applicant Device Name Decision Date
K161663 ENEURA INC sTMS mini 08/23/2016
K162797 eNeura Inc. SpringTMS 06/26/2017
DEN130022 ENEURA THERAPEUTICS NEURALIEVE CERENA TRANSCRANIAL MAGNETIC STIMULATOR 12/13/2013
K140094 ENEURA THERAPEUTICS, LLC SPRINGTMS TOTAL MIGRAINE SYSTEM 05/21/2014
K230358 eNeura, Inc. SAVI Dual (TM) Migraine Therapy 05/16/2023
K182976 eNeura« Inc. SpringTMS 02/25/2019


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