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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