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GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K954967
510(k) Type
Traditional
Applicant
GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1996
Days to Decision
168 days
Submission Type
Statement

GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K954967
510(k) Type
Traditional
Applicant
GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1996
Days to Decision
168 days
Submission Type
Statement