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GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993793
510(k) Type
Traditional
Applicant
GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2000
Days to Decision
64 days
Submission Type
Statement

GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993793
510(k) Type
Traditional
Applicant
GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2000
Days to Decision
64 days
Submission Type
Statement