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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrocautery, Gynecologic (And Accessories)
510(k) Number K931541
Device Name MODEL 26-0375, ELECTROSURGICAL GENERATOR
Applicant
CAMERON-MILLER, INC.
3949 SOUTH RACINE
CHICAGO,  IL  60609
Applicant Contact JOHN W MARTIN
Correspondent
CAMERON-MILLER, INC.
3949 SOUTH RACINE
CHICAGO,  IL  60609
Correspondent Contact JOHN W MARTIN
Regulation Number884.4120
Classification Product Code
HGI  
Date Received03/29/1993
Decision Date 06/01/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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