FDA 510(k) Applications Submitted by HONG DI PLASTIC PRODUCTS CO, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K102098 07/27/2010 POWDER FREE VINYL PATIENT EXAMINATION GLOVES HONG DI PLASTIC PRODUCTS CO, LTD.
K070187 01/22/2007 POWDER FREE VINYL PATIENT EXAMINATION GLOVE HONG DI PLASTIC PRODUCTS CO, LTD.
K070188 01/22/2007 POWDER FREE VINYL PATIENT EXAMINATION GLOVE, YELLOW HONG DI PLASTIC PRODUCTS CO, LTD.
K102099 07/27/2010 POWDER FREE VINYL PATIENT EXAMINATION GLOVES HONG DI PLASTIC PRODUCTS CO, LTD.


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