FDA 510(k) Applications Submitted by PT. MANDIRI INTI BUANA

FDA 510(k) Number Submission Date Device Name Applicant
K031020 03/31/2003 FLEXISKIN LATEX EXAMINATION GLOVES, POWDERED, NON STERILE PT. MANDIRI INTI BUANA
K031754 03/31/2003 FLEXISKIN POWDER FREE LATEX EXAMINATION GLOVES, NON STERILE PT. MANDIRI INTI BUANA
K042239 08/18/2004 FLEXISKIN POWDER FREE NITRILE EXAMINATION GLOVES, NON STERILE PT. MANDIRI INTI BUANA
K051987 07/22/2005 FLEXISKIN POLYMER COATED LATEX EXAMINATION GLOVES, POWDER FREE, NON-STERILE PT. MANDIRI INTI BUANA


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