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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Aversive Conditioning
510(k) Number K790738
Device Name HABITSABATER
Applicant
JACKSON ENT.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
JACKSON ENT.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number882.5235
Classification Product Code
HCB  
Date Received04/16/1979
Decision Date 06/20/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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