FDA 510(k) Applications Submitted by HIGH MOMENTUM SDN BHD

FDA 510(k) Number Submission Date Device Name Applicant
K060858 03/29/2006 LATEX POWDERED EXAMINATION GLOVE HIGH MOMENTUM SDN BHD
K071207 05/01/2007 MASTER GUARD NITRILE BLUE POWDERED EXAMINATION GLOVES HIGH MOMENTUM SDN BHD
K071208 05/01/2007 MASTER GUARD NITRILE BLUE POWDER FREE EXAMINATION GLOVES HIGH MOMENTUM SDN BHD
K071209 05/01/2007 MASTER GUARD LATEX POWDER FREE EXAMINATION GLOVES HIGH MOMENTUM SDN BHD


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