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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 # 30
Col. Florida
Mexico City Cp 01030,  MX
Applicant Contact SERGIO S CORDERO
Correspondent
S. Cordero Co.
2da Cerrada De Camelia # 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
Predetermined Change
Control Plan Authorized		 No
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