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FDA 510(k) Applications Submitted by ASSURGUARD SDN. BHD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K123760
12/07/2012
MULTIPLE NAME
ASSURGUARD SDN. BHD.
K123757
12/07/2012
POWDER FREE LATEX PATIENT EXAMINATION GLOVES, WITH PROTEIN CONTENT LABELING CLAIM, NATURAL COLOR
ASSURGUARD SDN. BHD.
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