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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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