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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tip, vessel
510(k) Number K791645
Device Name VICKERS MEDICAL MODEL 112 TREONIC DC2
Applicant
VICKERS AMERICA MEDICAL CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
VICKERS AMERICA MEDICAL CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.5540
Classification Product Code
FKW  
Date Received08/23/1979
Decision Date 10/02/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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