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FDA 510(k) Applications Submitted by WEI FANG JIUZHOU GLOVES CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060884
03/31/2006
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
WEI FANG JIUZHOU GLOVES CO., LTD.
K060886
03/31/2006
POWDERED VINYL PATIENT EXAMINATION GLOVES
WEI FANG JIUZHOU GLOVES CO., LTD.
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