Last synced on 25 January 2026 at 3:41 am

GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
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
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