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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name handle, scalpel
510(k) Number K863808
Device Name THE S. CORDERO STYLUS
Applicant
S. CORDERO CO.
2DA CERRADA DE CAMELIA NO. 30
COL. FLORIDA
MEXICO CITY CP 01030,  MX
Applicant Contact SERGIO S CORDERO
Correspondent
S. CORDERO CO.
2DA CERRADA DE CAMELIA NO. 30
COL. FLORIDA
MEXICO CITY CP 01030,  MX
Correspondent Contact SERGIO S CORDERO
Regulation Number878.4800
Classification Product Code
GDZ  
Date Received09/30/1986
Decision Date 10/14/1986
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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