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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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