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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Scissors, General, Surgical
510(k) Number K884095
Device Name SCISSORS, WIRE CUTTING
Applicant
Magnatrade Corp.
321 S. Boston, Suite 1050
Tulsa,  OK  74103
Applicant Contact MARC P BULLOCK
Correspondent
Magnatrade Corp.
321 S. Boston, Suite 1050
Tulsa,  OK  74103
Correspondent Contact MARC P BULLOCK
Regulation Number878.4800
Classification Product Code
LRW  
Date Received09/28/1988
Decision Date 10/19/1988
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
Predetermined Change
Control Plan Authorized		 No
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