FDA 510(k) Applications Submitted by ZIBO HENGDE PLASTIC & RUBBER PRODUCTS CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K070006 01/03/2007 POWDER-FREE VINYL PATIENT EXAMINATION GLOVES ZIBO HENGDE PLASTIC & RUBBER PRODUCTS CO., LTD.
K070008 01/03/2007 POWDERED VINYL PATIENT EXAMINATION GLOVES ZIBO HENGDE PLASTIC & RUBBER PRODUCTS CO., LTD.


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