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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 K871158
Device Name SIBIS REMOTE ACTUATOR
Applicant
HUMAN TECHNOLOGIES, INC.
1325 SNELL ISLE BLVD N.E.
ST. PETERSBURG,  FL  33704
Applicant Contact JAMES N DEERING
Correspondent
HUMAN TECHNOLOGIES, INC.
1325 SNELL ISLE BLVD N.E.
ST. PETERSBURG,  FL  33704
Correspondent Contact JAMES N DEERING
Regulation Number882.5235
Classification Product Code
HCB  
Date Received03/24/1987
Decision Date 05/29/1987
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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