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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tape, camera, surgical
510(k) Number K962148
Device Name VERGE VIDEOMETER
Applicant
VERG, INC.
633 WELLINGTON CRESCENT
WINNIPEG, MANITOBA,  CA R3M 0A8
Applicant Contact VERNON C TAYLOR
Correspondent
VERG, INC.
633 WELLINGTON CRESCENT
WINNIPEG, MANITOBA,  CA R3M 0A8
Correspondent Contact VERNON C TAYLOR
Regulation Number878.4160
Classification Product Code
FXN  
Date Received06/03/1996
Decision Date 12/20/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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