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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
510(k) Number K780954
Device Name SCISSORS, HOOK, ELECTROSURGICAL
Applicant
Kli
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Kli
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number884.4160
Classification Product Code
KNF  
Date Received06/09/1978
Decision Date 06/22/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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