Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

OMB · Predicate Candidate Screening

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

143 daysmedian FDA review time
299 days90th percentile
42clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K260998Ceribell Neurology Review SoftwareCeribell, Inc.2026-06-24900
K252070Ceribell Infant Seizure Detection SoftwareCeribell, Inc.2025-11-211430
K252160Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15Persyst Development, LLC2025-10-311130
K243743autoSCORE (V 2.0.0)Holberg Eeg AS2025-04-091260
K241589Ceribell Seizure Detection SoftwareCeribell, Inc.2025-04-093100
K242446Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15Persyst Development Corporation2025-01-221590
K241390NeuroMatchLVIS Corporation2024-11-261950
K240408REMI-AI Rapid Detection Module (REMI-AI RDM)Epitel, Inc.2024-10-172510
K240993encevis (2.1)Ait Austrian Institute of Technology GmbH2024-09-271690
K231068autoSCOREHolberg Eeg AS2024-01-072680
K231779REMI AI Discrete Detection ModuleEpitel, Inc.2024-01-032010
K222450LVIS NeuroMatchLVIS Corporation2023-06-092980
K223504Ceribell Status Epilepticus MonitorCeribell, Inc.2023-05-231820
K222002Persyst 15 EEG Review and Analysis SoftwarePersyst Development Corporation2022-12-301760
K211452EncevisAustrian Institute of Technology GmbH2021-12-022060
K200878Natus NeuroWorksNatus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)2020-05-18460
K191301Ceribell Pocket EEG DeviceCeribell, Inc.2019-09-111200
K182181Persyst 14 EEG Review and Analysis SoftwarePersyst Development Corporation2018-11-291080
K171720encevisAit Austrian Institute of Technology GmbH2018-04-193110
K180421Natus NeuroWorksNatus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)2018-03-14260
K171184Persyst Mobile AppPersyst Development Corporation2017-09-211500
K150688IdentEventOptima Neuroscience, Inc.2015-11-052330
K151929PERSYST 13 (P13) EEG REVIEW AND ANALYSIS SOFTWAREPersyst Development Corporation2015-08-12290
K141883CLINISCANSM EEGPicofemto, LLC2015-05-153080
K140552CADWELL SPIKE AND SEIZURE DETECTORCadwell2014-07-231410
K133793PERSYST 12 ( P12) EGG REVIEW AND ANALYSIS SOFTWAREPersyst Development Corporation2014-05-191570
K132306PERSYST 12 EEG REVIEW AND ANALYSIS SOFTWAREPersyst Development Corp.2013-11-211200
K120260ICTAExcel-Tech Ltd. (Xltek)2012-06-291540
K090019NATUS NEUROWORKS, MODEL 104196Natus Medical, Inc.2010-02-224160
K092039IDENTEVENT, VERSION 1.0GOptima Neuroscience, Inc.2009-10-161020
K042223XLTEK CONNEX IP HEADBOX, MODEL 1054Excel Tech. , Ltd.2004-09-16300
K011397PERSYST REVEALPersyst Development Corp.2001-08-03880
K010085EEG REAL PATIENT SPIKE AND EVENT DETECTOR MODULE, MODEL EX-SExcel Tech. , Ltd.2001-03-15630
K002332EEG SPIKE AND EVENT DETECTOR MODULEExcel Tech. , Ltd.2000-10-06660
K960273HARMONIE SENSAStellate Systems1996-04-04760
K955787DIGITRACE HOME VIDEO SYSTEMNew England Medical Instruments, Inc.1996-02-09500
K951594BIO-LOGIC AUTOMATIC EVENT ANALYSISBio-Logic Systems Corp.1995-08-221380
K950270NMI SOFTWARENicolet Biomedical, Inc.1995-05-151120
K944833DIGITRACE SLEEP COMPUTER, SLEEPPAC, HOME SLEEP SYSTEMNew England Medical Monitoring Co.1995-05-042160
K950117PERSYST SPIKE DETECTORPersyst Consulting Services, Inc.1995-04-05840
K910771DIGITRACE(TM) HOME MONIT COMP/ELB(TM) EEG LUNCH BXNew England Medical Instruments, Inc.1991-12-182990
K870450SZAC-16 SEIZURE ANALYSIS COMPUTERGrass-Telefactor Product Group1987-04-08640

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