Anesthesiology
Review Panel
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- ChemistryReview Panel
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- Gastroenterology and UrologyReview Panel
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- MiscellaneousMiscellaneous
- Subpart B—Cardiovascular Diagnostic DevicesCFR Sub-Part
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart B—Neurological Diagnostic DevicesCFR Sub-Part
- GXWEchoencephalograph2Product Code
- GXXBlock, Test, Ultrasonic Scanner Calibration1Product Code
- GXYElectrode, Cutaneous2Product Code
- GXZElectrode, Needle2Product Code
- GYATester, Electrode/Lead, Electroencephalograph1Product Code
- GXSMonitor, Alpha2Product Code
- GWEStimulator, Photic, Evoked Response2Product Code
- GWFStimulator, Electrical, Evoked Response2Product Code
- GWGEndoscope, Neurological2Product Code
- GWIDiscriminator, Two-Point1Product Code
- GWJStimulator, Auditory, Evoked Response2Product Code
- GWKConditioner, Signal, Physiological2Product Code
- GWLAmplifier, Physiological Signal2Product Code
- GWMDevice, Monitoring, Intracranial Pressure2Product Code
- GWNNystagmograph2Product Code
- GWQFull-Montage Standard Electroencephalograph2Product Code
- GWRGenerator, Electroencephalograph Test Signal1Product Code
- GWSAnalyzer, Spectrum, Electroencephalogram Signal1Product Code
- GWWAtaxiagraph1Product Code
- GWXFork, Tuning1Product Code
- GWYPinwheel1Product Code
- GWZPercussor1Product Code
- GXBEsthesiometer1Product Code
- GYBMedia, Electroconductive2Product Code
- GYCElectrode, Cortical2Product Code
- GYDTransducer, Tremor2Product Code
- GYEEncephalogram Telemetry System2Product Code
- GZKElectrode, Nasopharyngeal2Product Code
- GZLElectrode, Depth2Product Code
- GZMAnalyzer, Rigidity2Product Code
- GZNRheoencephalograph3Product Code
- GZODevice, Galvanic Skin Response Measurement2Product Code
- GZPStimulator, Mechanical, Evoked Response2Product Code
- HCJDevice, Skin Potential Measurement2Product Code
- HCSDevice, Temperature Measurement, Direct Contact, Powered2Product Code
- JXEDevice, Nerve Conduction Velocity Measurement2Product Code
- JXFPlethysmograph, Ocular3Product Code
- LLNDevice, Vibration Threshold Measurement1Product Code
- LQWTest, Temperature Discrimination1Product Code
- NCGNeuropsychiatric Interpretative Electroencephalograph Assessment Aid2Product Code
- NTUEvoked Potential Stimulator, Thermal2Product Code
- OLTNon-Normalizing Quantitative Electroencephalograph Software2Product Code
- OLUNormalizing Quantitative Electroencephalograph Software2Product Code
- OLVStandard Polysomnograph With Electroencephalograph2Product Code
- OLWIndex-Generating Electroencephalograph Software2Product Code
- OLXSource Localization Software For Electroencephalograph Or Magnetoencephalograph2Product Code
- OLYMagnetoencephalograph2Product Code
- OLZAutomatic Event Detection Software For Polysomnograph With Electroencephalograph2Product Code
- K242094Dreem 3S2Cleared 510(K)
- K233438SleepStageML2Cleared 510(K)
- K223539Dreem 3S2Cleared 510(K)
- K223922SOMNUM (V.1.1.2.)2Cleared 510(K)
- K221179SomnoMetry2Cleared 510(K)
- K210034EnsoSleep2Cleared 510(K)
- K202142Sleepware G32Cleared 510(K)
- K192469Nox Sleep System2Cleared 510(K)
- K182227Esprit Nova2Cleared 510(K)
- K173366NicoletOne2Cleared 510(K)
- K163617REMbrandt2Cleared 510(K)
- K162627EnsoSleep2Cleared 510(K)
- K162140RemLogic2Cleared 510(K)
- K153353SANDMAN ELITE2Cleared 510(K)
- K153412Sleep Profiler2Cleared 510(K)
- K142988Sleepware G32Cleared 510(K)
- K142825Zmachine2Cleared 510(K)
- K130007SLEEP PROFILER2Cleared 510(K)
- K120450SLEEP PROFILER2Cleared 510(K)
- K090277NATUS SLEEPWORKS, MODEL 1040172Cleared 510(K)
- K062943POLYSMITH SLEEP SYSTEM, MODEL NTI54982Cleared 510(K)
- K040595ALICE 52Cleared 510(K)
- K002622BIOSLEEP2Cleared 510(K)
- K963631SLEEP STUDY ANALYSIS (SSA) VERSION 96.102Cleared 510(K)
- K961636MEDILOG VISION2Cleared 510(K)
- K915856SENSORMEDICS 4000 SERIES SLEEP SYSTEM2Cleared 510(K)
- K894155SLEEPSCAN2Cleared 510(K)
- K891383MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM2Cleared 510(K)
- K890513SAC 747 AND SAC 847 (SLEEP ANALYZING COMPUTERS)2Cleared 510(K)
- K871990MODEL MPA MULTI PARAMETER ANALYSIS MONITORING SYS.2Cleared 510(K)
- K862527SLEEP ANALYZING COMPUTER2Cleared 510(K)
- OMAAmplitude-Integrated Electroencephalograph2Product Code
- OMBAutomatic Event Detection Software For Full-Montage Electroencephalograph2Product Code
- OMCReduced- Montage Standard Electroencephalograph2Product Code
- ORTBurst Suppression Detection Software For Electroencephalograph2Product Code
- PIWBrain Injury Adjunctive Interpretive Electroencephalograph Assessment Aid2Product Code
- PKQComputerized Cognitive Assessment Aid2Product Code
- PNAEvoked Photon Image Capture Device1Product Code
- POMComputerized Cognitive Assessment Aid For Concussion2Product Code
- POPCranial Motion Measurement Device2Product Code
- POSPhysiological Signal Based Seizure Monitoring System2Product Code
- PSPIntracranial Pressure & Temperature Monitoring Kit2Product Code
- PTBAtaxiagraph With Interpretive Software1Product Code
- PTYComputerized Cognitive Assessment Aid, Exempt2Product Code
- PVPNeurological Test Kit1Product Code
- QEABrain Injury Adjunctive Interpretive Oculomotor Assessment Aid2Product Code
- QPFPediatric Autism Spectrum Disorder Diagnosis Aid2Product Code
- OPTInfrared Hematoma Detector2Product Code
- Subpart B—Physical Medicine Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart D—Physical Medicine Prosthetic DevicesCFR Sub-Part
- Subpart E—Neurological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—Cardiovascular Therapeutic DevicesCFR Sub-Part
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
- PathologyReview Panel
- Physical MedicineReview Panel
- RadiologyReview Panel
- General and Plastic SurgeryReview Panel
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
Zmachine
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K142825
- 510(k) Type
- Traditional
- Applicant
- CONSOLIDATED RESEARCH OF RICHMOND, INC
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 1/20/2015
- Days to Decision
- 112 days
- Submission Type
- Summary