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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 K851751
Device Name 7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1
Applicant
ARTIBERIA
4518 LOS RANCHITOS
SAN ANTONIO,  TX  78233
Applicant Contact GIL M SANCHEZ
Correspondent
ARTIBERIA
4518 LOS RANCHITOS
SAN ANTONIO,  TX  78233
Correspondent Contact GIL M SANCHEZ
Regulation Number878.4800
Classification Product Code
GDX  
Date Received04/25/1985
Decision Date 06/20/1985
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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