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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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