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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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