FDA 510(k), K110268, FORCETRIAD ELECTROSURGICAL GENERATOR

FDA 510(k), K110268, FORCETRIAD ELECTROSURGICAL GENERATOR

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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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