Medical Device Manufacturer · US , Malvern , PA

Neuronetics - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 2008
7
Total
6
Cleared
1
Denied

Neuronetics has 6 FDA 510(k) cleared medical devices. Based in Malvern, US.

Last cleared in 2023. Active since 2008. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Neuronetics Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Neuronetics

7 devices
1-7 of 7
Cleared Dec 13, 2023
NeuroStar Advanced Therapy System (Version 3.8)
K233621 · OBP
Neurology · 30d
Cleared Jun 08, 2023
OCD MT Cap (85-00397-000)
K231350 · QCI
Neurology · 30d
Cleared Apr 04, 2023
NeuroStar Advanced Therapy System (Version 3.7)
K230029 · OBP
Neurology · 90d
Cleared Mar 28, 2014
NEUROSTAR TMS THERAPY SYSTEM
K133408 · OBP
Neurology · 142d
Cleared Apr 30, 2013
NEUROSTAR TMS THERAPY SYSTEM
K130233 · OBP
Neurology · 90d
Cleared Dec 16, 2008
NEUROSTAR TMS THERAPY SYSTEM, MODEL 1.1
K083538 · OBP
Neurology · 18d
Not Cleared Oct 07, 2008
NEUROSTAR TMS SYSTEM
DEN070003 · OBP
Neurology · 502d
Filters
Filter by Specialty
All7 Neurology 7