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HYCARE LATEX EXAMINATION GLOVE, POWDERED

Page Type
Cleared 510(K)
510(k) Number
K010875
510(k) Type
Traditional
Applicant
HYCARE INTL. CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2001
Days to Decision
76 days
Submission Type
Statement

HYCARE LATEX EXAMINATION GLOVE, POWDERED

Page Type
Cleared 510(K)
510(k) Number
K010875
510(k) Type
Traditional
Applicant
HYCARE INTL. CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2001
Days to Decision
76 days
Submission Type
Statement