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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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