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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Scalpel, One-Piece
510(k) Number K921167
Device Name ULTRABLADE
Applicant
MICRON TECHNOLOGY, INC.
CENTENNIAL CREEK OFFICE PARK
2975 VALMONT AVE., SUITE 310
BOULDER,  CO  80301
Applicant Contact RICHARD ROSENTHAL
Correspondent
MICRON TECHNOLOGY, INC.
CENTENNIAL CREEK OFFICE PARK
2975 VALMONT AVE., SUITE 310
BOULDER,  CO  80301
Correspondent Contact RICHARD ROSENTHAL
Regulation Number878.4800
Classification Product Code
GDX  
Date Received03/11/1992
Decision Date 07/30/1992
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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