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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 K924469
Device Name GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR)
Applicant
Conmedcorp
310 Broad St.
Utica,  NY  13501 -1203
Applicant Contact MARTIN P FORTE
Correspondent
Conmedcorp
310 Broad St.
Utica,  NY  13501 -1203
Correspondent Contact MARTIN P FORTE
Regulation Number878.4400
Classification Product Code
GEI  
Date Received09/02/1992
Decision Date 04/07/1993
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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