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FDA 510(k) Applications Submitted by GREAT GLOVE SDN BHD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K993386
10/08/1999
LATEX EXAMINATION POWDERED GLOVES
GREAT GLOVE SDN BHD
K052955
10/21/2005
NITRILE BLUE POWDERED EXAMINATION GLOVES
GREAT GLOVE SDN BHD
K052956
10/21/2005
NITRILE BLUE POWDER FREE EXAMINATION GLOVE
GREAT GLOVE SDN BHD
K020363
02/04/2002
GREAT GLOVE LATEX EXAMINATION POWDERFREE GLOVES WITH PROTEIN LABELLING CLAIMS (50 MICROGRAMS OR LESS)
GREAT GLOVE SDN BHD
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