FDA 510(k) Applications Submitted by KOSSAN LATEX INDUSTRIES(M)SDN BHD

FDA 510(k) Number Submission Date Device Name Applicant
K123749 12/06/2012 POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, GREEN, NON-STERILE KOSSAN LATEX INDUSTRIES(M)SDN BHD
K120066 01/09/2012 POWDER FREE NITRILE PATIENT EXAMINATION GLOVE, BLUE, WHITE AND GREEN COLORED. NON-STERILE, LOW DERMATITIS POTENTIAL KOSSAN LATEX INDUSTRIES(M)SDN BHD
K111772 06/23/2011 POWDER FREE NITRILE PATIENT EXAMINATION GLOVE, BLUE COLORED AND WHITE (NON-COLORED). NON-STERILE KOSSAN LATEX INDUSTRIES(M)SDN BHD
K062764 09/15/2006 POWDER-FREE NITRILE PATIENT EXAMINATION GLOVE, WHITE (NON-COLORED) AND BLUE COLORED KOSSAN LATEX INDUSTRIES(M)SDN BHD


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