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GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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