FDA 510(k) Applications for Medical Device Product Code "MUK"

FDA 510(k) Number Applicant Device Name Decision Date
K020126 SURX, INC. MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM) 03/15/2002
K011190 SURX, INC. SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM) 01/08/2002
K020952 SURX, INC. SURX RF SYSTEM 05/30/2002


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