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FDA 510(k) Applications Submitted by Neuronetics
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230029
01/04/2023
NeuroStar Advanced Therapy System (Version 3.7)
Neuronetics
K231350
05/09/2023
OCD MT Cap (85-00397-000)
Neuronetics
DEN070003
05/24/2007
NEUROSTAR TMS SYSTEM
NEURONETICS
K083538
11/28/2008
NEUROSTAR TMS THERAPY SYSTEM, MODEL 1.1
NEURONETICS
K130233
01/30/2013
NEUROSTAR TMS THERAPY SYSTEM
NEURONETICS
K133408
11/06/2013
NEUROSTAR TMS THERAPY SYSTEM
NEURONETICS
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