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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 K040638
Device Name VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2
Applicant
VNUS MEDICAL TECHNOLOGIES, INC.
750 CHESAPEAKE DR.
REDWOOD CITY,  CA  94063
Applicant Contact SAM NANAVATI
Correspondent
VNUS MEDICAL TECHNOLOGIES, INC.
750 CHESAPEAKE DR.
REDWOOD CITY,  CA  94063
Correspondent Contact SAM NANAVATI
Regulation Number878.4400
Classification Product Code
GEI  
Date Received03/10/2004
Decision Date 06/07/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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