510(k) K183692

Device
Avid IF2
Applicant
Vision Quest Industries Inc./ Dba VQ OrthoCare
510(k) number
K183692
Product code
LIH  
Decision
Substantially Equivalent (SESE)
Decision date
2019-06-12
Date received
2018-12-31
Regulation
882.5890
Classification name
Interferential Current Therapy
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Mohamed Ouerghi
Address
1390 Decision St., Suite A Vista CA US 92081 92081

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code LIH  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K231575Vecttor VT-300Artaflex, Inc.2024-02-08
K202725ETD4000Therasigma, LLC2021-03-26
K122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.2012-12-21
K121662VECTTOR VT-200Alan Neuromedical Technologies, LLC2012-11-21
K110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd2011-06-20
K100246MAX-IF1000Bio Protech, Inc.2010-11-24
K092780INF 4160 PLUS, MODEL D-FJ31FFuji Dynamics Limited2010-01-07
K092763IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206DWell-Life Healthcare Limited2009-10-08
K090023IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR, MODEL: WL-2206B AND WL-2106EWell-Life Healthcare Limited2009-01-30
K070890EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507Everlife Medical Equipment Co., Ltd.2007-06-29
K060975IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2Theratech, Inc.2006-05-10
K052289DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICEBiowave Corporation2005-12-13
K043407INF 4160, MODEL D-FJ27FFuji Dynamics Limited2005-02-11
K042057INFINITY ELECTROTHERAPY SYSTEMEmpi2004-12-17
K040007INTERFERENTIAL STIMULATOR, MODEL BMLS02-6Biomedical Life Systems, Inc.2004-07-07

Legacy Summary#

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FDA Review#

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