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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Media, Electroconductive
510(k) Number K841871
Device Name LIQUA-SONIC GEL
Applicant
Chester Labs, Inc.
3208 Dixie Hwy.
Erlanger,  KY  41018
Applicant Contact HOWARD NEWTON
Correspondent
Chester Labs, Inc.
3208 Dixie Hwy.
Erlanger,  KY  41018
Correspondent Contact HOWARD NEWTON
Regulation Number882.1275
Classification Product Code
GYB  
Date Received05/07/1984
Decision Date 03/14/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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