FDA 510(k) Applications Submitted by ULTRAWIN SDN BHD

FDA 510(k) Number Submission Date Device Name Applicant
K090828 03/26/2009 NON-STERILE, POWDER FREE NITRILE EXAMINATION GLOVES ULTRAWIN SDN BHD
K992175 06/28/1999 EXTRA-CARE LATEX PATIENT EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED ULTRAWIN SDN BHD
K983175 09/10/1998 EXTRA-CARE POWDER-FREE EXAMINATION GLOVE ULTRAWIN SDN BHD
K072802 10/01/2007 SINGLE USE, DISPOSABLE, BLUE COLOR, POWDER FREE LATEX PATIENT EXAMINATION GLOVE ULTRAWIN SDN BHD


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