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FDA 510(k), K052003, VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS FLEX, MODEL RFX-6-XX (XX = 10, 20, 30 & 40)
FDA 510(k), K052003, VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS FLEX, MODEL RFX-6-XX (XX = 10, 20, 30 & 40)
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510(K) Number: K052003
Device Name: VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS FLEX, MODEL RFX-6-XX (XX = 10, 20, 30 & 40)
Manufacturer: VNUS MEDICAL TECHNOLOGIES, INC.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 07/25/2005
Decision Date: 10/11/2005
Regulation Medical Specialty: General & Plastic Surgery
Device Name: VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS FLEX, MODEL RFX-6-XX (XX = 10, 20, 30 & 40)
Manufacturer: VNUS MEDICAL TECHNOLOGIES, INC.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 07/25/2005
Decision Date: 10/11/2005
Regulation Medical Specialty: General & Plastic Surgery
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