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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 K861372
Device Name ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORY
Applicant
Snowden-Pencer
6191 Atlantic Blvd.
Norcross,  GA  30071
Applicant Contact NORMAN BLACK
Correspondent
Snowden-Pencer
6191 Atlantic Blvd.
Norcross,  GA  30071
Correspondent Contact NORMAN BLACK
Regulation Number878.4400
Classification Product Code
GEI  
Date Received04/11/1986
Decision Date 06/19/1986
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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