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FDA 510(k) Applications Submitted by LANGFANG HUILONG PLASTIC PRODUCT CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K071685
06/20/2007
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
LANGFANG HUILONG PLASTIC PRODUCT CO., LTD.
K071686
06/20/2007
POWDERED VINYL PATIENT EXAMINATION GLOVES
LANGFANG HUILONG PLASTIC PRODUCT CO., LTD.
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