FDA 510(k) Applications Submitted by TOP CALIBRE SDN BHD

FDA 510(k) Number Submission Date Device Name Applicant
K123819 12/12/2012 MULTIPLE NAME TOP CALIBRE SDN BHD
K133949 12/23/2013 POWDER FREE NITRILE PATIENT EXAMINATION GLOVE,BLUE AND ORANGE COLORED,NON-STERILE TESTED FOR USE WITH CHEMOTHERAPY DRUGS TOP CALIBRE SDN BHD
K120692 03/07/2012 LATEX EXAMINATION GLOVES (POWDER FREE) TOP CALIBRE SDN BHD
K120693 03/07/2012 LATEX EXAMINATION GLOVES (POWDERED) TOP CALIBRE SDN BHD
K112612 09/07/2011 POWDER FREE LATEX PATIENT EXAMINATION GLOVE, WITH PROTEIN CONTENT LABELING CLAIM TOP CALIBRE SDN BHD


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