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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Interferential Current Therapy
510(k) Number K183692
Device Name Avid IF2
Applicant
Vision Quest Industries Inc./Dba VQ Orthocare
1390 Decision St., Suite A
Vista,  CA  92081
Applicant Contact Mohamed Ouerghi
Correspondent
Vision Quest Industries Inc./Dba VQ Orthocare
1390 Decision St., Suite A
Vista,  CA  92081
Correspondent Contact Mohamed Ouerghi
Regulation Number882.5890
Classification Product Code
LIH  
Date Received12/31/2018
Decision Date 06/12/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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