FDA 510(k) Applications Submitted by SHANGHAI GIANTMAX PLASTIC PRODUCT CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K032745 09/04/2003 SHANGHAI GIANTMAX POWDERED CLEAR VINYL EXAMINATION GLOVES SHANGHAI GIANTMAX PLASTIC PRODUCT CORP.
K032746 09/04/2003 SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES SHANGHAI GIANTMAX PLASTIC PRODUCT CORP.


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