Atlas FDA

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

GWE — Predicate Candidate Screening

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

115 daysmedian FDA review time
432 days90th percentile
49clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K221471E3 and ProfileDiagnosys, LLC2022-11-221860
K212936Vision Monitor- MonCvONEMetrovision2022-11-214320
K211974LED PHOTIC SystemMicromed S.P.A.2021-09-23900
K211643Vision Monitor - MonpackONEMetrovision2021-07-26600
K200705Nurochek SystemCryptych Pty, Ltd.2020-04-23360
K173936Natus Photic StimulatorNatus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)2018-06-151710
K142567RETeval Visual Electrodiagnostic DeviceLkc Technologies, Inc.2015-05-192490
K113785ADHERENT VISUAL STIMULATOR GOGGLESAnschel Technology, Inc.2012-06-061660
K120104VISIONSEARCH 1Visionsearch Pty, Ltd.2012-05-211290
K101763DIOPSYS NOVA VEP VISION TESTING SYSTEMDiopsys, Inc.2011-05-093200
K101691LIFELINES PHOTIC STIMULATORLifelines , Ltd.2010-08-10550
K081591NEUCODIAVerisci Corporation2009-05-153430
K043367GLAID OCULAR ELECTROPHYSIOLOGY DEVICELace Electronica S.R.L.2005-11-173440
K043491ENFANTTMDiopsys, Inc.2005-03-16891
K023525RETISCAN, RETIPORTRoland Consult2004-03-265220
K022304ACCUMAP AUTOMATIC PERIMETERObjectivision Pty , Ltd.2003-11-144860
K011794XLTEK LED GOGGLES, MODEL LED-01Excel Tech. , Ltd.2001-10-011150
K001467DA VINCHI EMG/EP ISA1004EPAirsep Corp.2000-08-01830
K991903EXCEL PHOTIC STIMULATOR, MODEL (XLPS-1)Excel Tech. , Ltd.1999-08-04610
K971214KILOWINCadwell Laboratories, Inc.1998-06-114350
K932571TOMEY PE-400 PORTABLE ERG & VEP WITH OPTIONAL PS-4Tomey Corporation USA1995-08-318260
K903734ADVANTAGE EPClark Davis Medical Systems, Inc.1991-07-223400
K883914FATIGMETERK. Jimbo Co., Inc.1989-10-314100
K880593TECA/MEDELEC MISTRALTeca, Inc.1988-04-06550
K874136PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTALBio-Logic Systems Corp.1988-03-251640
K872725MODEL 100 VISUAL EVOKED RESPONSE RECORDING SYSTEMEyetronics, Inc.1987-08-14370
K861069TECA NEUROPTO WITH OS-5 STIMULATORTeca, Inc.1987-01-273130
K860910V100 VISUALLY EVOKED POTENTIAL MONITORNew Potentials, Inc.1986-12-182820
K860801MODEL 8400 W/MODIFICATIONS (SPECTRUM 32)Cadwell Laboratories, Inc.1986-11-182590
K863956MACULOSCOPE(TM)Doran Instruments, Inc.1986-11-13340
K854362MODIFIED BRAIN ATLAS IIIBio-Logic Systems Corp.1986-04-221750
K852533L.E.D. GOGGLES, MODEL 580-LEDGOGBio-Logic Systems Corp.1985-12-121810
K853412WAVE GATEWolfline Corp.1985-10-28760
K844659VPS 2250, CSU2250 & VFU 2250Madsen Electronics (Canada) , Ltd.1985-02-25910
K844616SIEGEN VISUAL STIMULATORSiegen Corp.1985-02-14790
K842964PHOTIC STIMULATOR TM-3030-70Tracor Northern, Inc.1984-12-281540
K842381SLS 3500 LED VISUAL STIMULATORNihon Kohden America, Inc.1984-11-091440
K834442LED STIMULATOR LS-05Teca, Inc.1984-08-082360
K831651EVOKED POTENTIAL SYSTEM 2000Ophthalmetric Corp.1983-09-121120
K832084EVOKED 3500 POTENTIAL SYSTEMTracor Northern, Inc.1983-08-16490
K831047BIOLOGIC SYSTEM BL 101Bio-Logic Systems Corp.1983-05-13430
K812061MODEL S10VS VISUAL STIMULATORGrass Instrument Co.1981-08-20300
K810481VISUAL PATTERN REVERSAL GEN. & PHOTIC S.Amplaid USA, Inc.1981-03-11160
K801671ESG-1 (EVOKED RESPONSE STIMULUS GENER)Neurodiagnostics, Inc.1980-08-04130
K791149STIMULATOR MODEL SSS-1101Nihon Kohden America, Inc.1979-09-17940
K790570STIMULATOR, NIC-106 VISUALNicolet Biomedical Instruments1979-05-23610
K790217GENERATOR, MODEL VG-1Street Electronics Corp.1979-02-0670
K781461MODEL 7320 VISUAL STIMULATORLife-Tech Instruments, Inc.1978-11-08820
K781398TECA VS6 VIDEO STIMULATORTeca, Inc.1978-08-2380

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