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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrosurgical Device
510(k) Number K932345
Device Name TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USE
Applicant
Conmedcorp
310 Broad St.
Utica,  NY  13501
Applicant Contact MARTIN FORTE
Correspondent
Conmedcorp
310 Broad St.
Utica,  NY  13501
Correspondent Contact MARTIN FORTE
Regulation Number878.4400
Classification Product Code
DWG  
Date Received05/14/1993
Decision Date 04/12/1994
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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