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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name stimulator, nerve, transcutaneous, over-the-counter
510(k) Number K170659
Device Name IQ Technologies
IQ Technologies Inc.
6672 Spencer St., Ste 800
Las Vegas,  NV  89119
Applicant Contact Elli Josef
Dr Certification LLC
1142 S. Diamond Bar Blvd, #861
Diamond Bar,  CA  91765
Correspondent Contact Bill Quanqin Dai
Regulation Number882.5890
Classification Product Code
Subsequent Product Code
Date Received03/03/2017
Decision Date 05/26/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No