FDA 510(k) Applications Submitted by HYCARE INTL. CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K020042 01/07/2002 HYCARE LATEX EXAMINATION GLOVE, POWDER FREE HYCARE INTL. CO., LTD.
K022530 07/31/2002 POWDERED LATEX EXAM GLOVES WITH PROTEIN LABELING (200UG/G OR LESS) HYCARE INTL. CO., LTD.
K010875 03/23/2001 HYCARE LATEX EXAMINATION GLOVE, POWDERED HYCARE INTL. CO., LTD.


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