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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K991814
Device Name MULTACHOICE INSTRUMENTS
Applicant
Dexide, Inc.
7509 Flagstone Dr.
Fort Worth,  TX  76118 -6995
Applicant Contact JOHN CORZINE
Correspondent
Dexide, Inc.
7509 Flagstone Dr.
Fort Worth,  TX  76118 -6995
Correspondent Contact JOHN CORZINE
Regulation Number878.4400
Classification Product Code
GEI  
Date Received05/27/1999
Decision Date 06/23/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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