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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