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FDA 510(k) Applications Submitted by SUPERMAX PLASTIC PRODUCTS CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K093797
12/10/2009
POWDER FREE VINYL PATIENT EXAMINATION GLOVES (YELLOW, WHITE)
SUPERMAX PLASTIC PRODUCTS CO., LTD.
K093798
12/10/2009
POWDER FREE VINYL PATIENT EXAMINATION GLOVE
SUPERMAX PLASTIC PRODUCTS CO., LTD.
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