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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