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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 K915204
Device Name MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT
Applicant
Conmedcorp
310 Broad St.
Utica,  NY  13501
Applicant Contact FORTE, JR.
Correspondent
Conmedcorp
310 Broad St.
Utica,  NY  13501
Correspondent Contact FORTE, JR.
Regulation Number878.4400
Classification Product Code
GEI  
Date Received11/18/1991
Decision Date 06/04/1992
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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