Medical Device Manufacturer · US , Cleveland Heights , OH

Neurowave Systems, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2010
3
Total
3
Cleared
0
Denied

Neurowave Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Cleveland Heights, US.

Last cleared in 2021. Active since 2010. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Neurowave Systems, Inc. Filter by specialty or product code using the sidebar.

1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Neurowave Systems, Inc.
3 devices
1-3 of 3
Cleared CT Aug 05, 2021
NeuroSENSE Monitoring System, Model NS-901
K202621 · OLW
Anesthesiology · 329d
Cleared Jun 23, 2015
DiscoverEEG System, Model DE-401
K142834 · OLT
Neurology · 266d
Cleared Oct 29, 2010
NeuroWave NeuroFAST MONITORING SYSTEM, MODEL NF-701
K092477 · OMC
Neurology · 443d
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All3 Neurology 2 Anesthesiology 1