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FDA 510(k) K110268, FORCETRIAD ELECTROSURGICAL GENERATOR, by Covidien Lp, Formerly Know AS Valleylab, A Divison

FDA 510(k) K110268, FORCETRIAD ELECTROSURGICAL GENERATOR, by Covidien Lp, Formerly Know AS Valleylab, A Divison

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510(K) Number: K110268
Device Name: FORCETRIAD ELECTROSURGICAL GENERATOR
Manufacturer: Covidien Lp, Formerly Know AS Valleylab, A Divison
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 01/28/2011
Decision Date: 05/31/2011
Regulation Medical Specialty: General & Plastic Surgery
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