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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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