ClearanceBrief
Company ยท US

Neurosoft, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2022. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OLTNon-Normalizing Quantitative Electroencephalograph Software2
OLXSource Localization Software For Electroencephalograph Or Magnetoencephalograph2
GWFStimulator, Electrical, Evoked Response1
IKNElectromyograph, Diagnostic1
JXEDevice, Nerve Conduction Velocity Measurement1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 30, 2022K220254Neuron-Spectrum-AM with Neuron-Spectrum.NET Software
Neurosoft , Ltd., RU
OLT
May 22, 2021K190703Neuro-IOM system with Neuro-IOM.NET software
Neurosoft , Ltd., RU
GWF
Jun 19, 2015K133995NEURON-SPECTRUM-4/P WITH NEURON-SPECTRUM.NET SOFTWARE
Neurosoft , Ltd., IT
OLT
Sep 19, 2001K011241NEUROSOFT'S SOURCE
Neurosoft, Inc.
OLX
Feb 5, 2001K001781CURRY MULTIMODAL NEUROIMAGING SOFTWARE
Neurosoft, Inc.
OLX
Nov 24, 2000K001692NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8
Neurosoft, Inc.
JXE
May 17, 2000K000812NEURO SCAN MEDICAL SYSTEMS, MODELS 302L MEDICOR (LABORATORY) AND 302P ADVANTAGE 3000 (PORTABLE)
Neurosoft, Inc.
IKN

Latest recalls

DateFirm and productCodeLinked 510(k)
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