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FDA 510(k), K083856, INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026
FDA 510(k), K083856, INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026
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510(K) Number: K083856
Device Name: INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026
Manufacturer: RELIEVANT MEDSYSTEMS, INC.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 12/24/2008
Decision Date: 01/22/2009
Regulation Medical Specialty: General & Plastic Surgery
Device Name: INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026
Manufacturer: RELIEVANT MEDSYSTEMS, INC.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 12/24/2008
Decision Date: 01/22/2009
Regulation Medical Specialty: General & Plastic Surgery
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