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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 Street, Suite A
Vista,  CA  92081
Applicant Contact Mohamed Ouerghi
Correspondent
Vision Quest Industries Inc./ dba VQ OrthoCare
1390 Decision Street, 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
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