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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrode, Depth
510(k) Number K891920
Device Name AD-TECH'S DEPTH ELECTRODE
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
1901 WILLIAM ST.
RACINE,  WI  53404 -1876
Applicant Contact ANTHONY PUTZ
Correspondent
AD-TECH MEDICAL INSTRUMENT CORP.
1901 WILLIAM ST.
RACINE,  WI  53404 -1876
Correspondent Contact ANTHONY PUTZ
Regulation Number882.1330
Classification Product Code
GZL  
Date Received03/27/1989
Decision Date 07/27/1989
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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