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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 K935490
Device Name ELECTROSURGICAL DEVICE, MODEL 26-2500
Applicant
Cameron-Miller, Inc.
3949 S. Racine
Chicago,  IL  60609
Applicant Contact JOHN W MARTIN
Correspondent
Cameron-Miller, Inc.
3949 S. Racine
Chicago,  IL  60609
Correspondent Contact JOHN W MARTIN
Regulation Number878.4400
Classification Product Code
GEI  
Date Received11/15/1993
Decision Date 04/01/1994
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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