Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

OLV — Predicate Candidate Screening

64 FDA 510(k) clearances under this product code; the 50 most recent screened below.

88 daysmedian FDA review time
245 days90th percentile
64clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K260585Noxturnal WebNox Medical Ehf2026-03-20280
K242447Falcon HSTCompumedics Limited2025-02-201880
K241288Noxturnal WebNox Medical Ehf2024-12-232300
K240700HomeSleepTest (HST, HST REM+)Somnomedics GmbH2024-12-082690
K213007Cerebra Sleep SystemCerebra Medical , Ltd.2022-07-062890
K201054SOMNOscreen plusSomnomedics GmbH2020-08-121130
K192624ApneaTrakCadwell Industries, Inc.2020-02-201500
K181709Serenity Piezo Sensor, Serenity Thermocouple SensorNeurotronics, Inc.2018-11-161410
K173868Serenity Body Position Sensor, Serenity RIP SensorsNeurotronics, Inc.2018-07-021940
K173690Grass TWinNatus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)2018-03-09980
K172986Zmachine SynergyConsolidated Research of Richmond, Inc. Dba General Sleep CO2017-12-19830
K172711Comet-PLUSNatus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)2017-11-03560
K161650Polysmith Sleep System, Model NTI7593Neurotronics, Inc.2017-01-192180
K142774Polysmith Sleep SystemNeurotronics, Inc.2015-02-181450
K131415LIVE VIEW PANEL (LVP)Neurotronics, Inc.2013-08-09850
K111055GALAXY SYSTEM; JUPITERPersonal Health Institute International2011-12-212500
K101830ZMACHINE, MODEL DT-100Consolidated Research of Richmond, Inc.2011-03-312730
K093728BE MICRO, TREAEb Neuro S.P.A.2010-04-291470
K073491EEG-1100A SWITCH BOXNihon Kohden America, Inc.2008-01-11300
K071782MICROMED BRAIN SPY PLUS, EMBIA TITANIUM DEVICESMicromed S.P.A.2008-01-101920
K050425AURA-PSGAstro-Med, Inc.2005-10-202440
K052066CEEGRAPH/SLEEPSCAN NETLINK TRAVELERBio-Logic Systems Corp.2005-08-26252
K050833ELECTRODE JUNCTION BOX, MODEL JE-921ANihon Kohden America, Inc.2005-04-29280
K050143OMNIPRO SYSTEMMays and Associates, Inc.2005-02-01110
K042039FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,Cleveland Medical Devices, Inc.2004-11-171110
K042364PANBUS DIGITAL EEG & SLEEP ACQUISITION DEVICESLamont Medical, Inc.2004-09-30300
K033475WIRELESS INPUT UNIT, MODEL WEE-1000A SERIESNihon Kohden America, Inc.2004-01-07650
K031202MEDIPALM-20Braebon Medical Corp.2003-05-01150
K022249NIGHTRON POLYSOMNOGRAPHY SYSTEMTelediagnostic Systems, Inc.2002-12-311720
K022037XLTEK SLEEP SYSTEMExcel Tech. , Ltd.2002-09-10780
K021807GRASS-TELEFACTOR AS40 AMPLIFIER SYSTEMGrass Instrument Co.2002-08-29870
K022121PSG INPUT BOX, MODEL JE-912AKNihon Kohden America, Inc.2002-07-29280
K021185NERVUS MONITORTaugagreining HF2002-07-12881
K012976TWIN PLUSGrass-Telefactor Divison2002-02-121600
K013450NOTTA AMBULATORY RECORDERStellate Systems2002-01-14890
K012085SOMNO STAR & SERIES SLEEP SYSTEMSensor Medics Corp.2001-08-02300
K010728HARMONE-SCHWARZER EEG SYSTEMStellate Systems2001-05-21701
K010460LIFELINES TRACKITLifelines , Ltd.2001-05-14870
K011204NEUROFAX, MODELS EEG-1100A, EEG-9100ANihon Kohden America, Inc.2001-05-08190
K003175COMPUMEDICS SIESTA SYSTEMCompumedics Limited2000-12-27780
K003681BIO-LOGIC SLEEPSCAN NETLINKBio-Logic Systems Corp.2000-12-21210
K001013MONET ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHYAirsep Corp.2000-05-16480
K000338VITAPORT 3Nihon Kohden America, Inc.2000-04-26830
K994142GRASS TS3201/6401 EEG AMPLIFIER SYSTEMGrass Instrument Co.2000-03-06890
K992742NEUROFAX, MODEL EEG-1100ANihon Kohden America, Inc.1999-10-14590
K992283ARTISAN ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHYAirsep Corp.1999-08-27510
K992291H20- TETHERED OPTIONGrass-Telefactor Product Group1999-08-06300
K991446BIOSACA SYSTEM, MODEL 800Biosys AB (Publ)1999-07-23880
K991900XLTEK POLYSOMNOGRAPHY HEADBOX, MODEL # PSG-40Excel Tech. , Ltd.1999-07-12380
K990522WARATAH DIGITAL EEG AND SLEEP ACQUISITION DEVICES WITH, OR WLamont Medical, Inc.1999-05-19900

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda