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POWDERFREE NITRILE PATIENT EXMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003985
510(k) Type
Traditional
Applicant
GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2001
Days to Decision
45 days
Submission Type
Statement

POWDERFREE NITRILE PATIENT EXMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003985
510(k) Type
Traditional
Applicant
GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2001
Days to Decision
45 days
Submission Type
Statement