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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name cannula, surgical, general & plastic surgery
510(k) Number K843187
Device Name CANNULA
Applicant
ETHICON, INC.
P.O BOX 151, ROUTE 22 WEST
SOMERVILLE,  NJ  08876
Applicant Contact ROBERT H O'HOLLA
Correspondent
ETHICON, INC.
P.O BOX 151, ROUTE 22 WEST
SOMERVILLE,  NJ  08876
Correspondent Contact ROBERT H O'HOLLA
Regulation Number878.4800
Classification Product Code
GEA  
Date Received08/13/1984
Decision Date 10/31/1984
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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