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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