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GUTHRIE LATEX SURGICAL GLOVE (PRE-POWDERED)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001047
510(k) Type
Traditional
Applicant
Guthrie Medicare Products (Melaka) Sdn Bhd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2000
Days to Decision
28 days
Submission Type
Statement

GUTHRIE LATEX SURGICAL GLOVE (PRE-POWDERED)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001047
510(k) Type
Traditional
Applicant
Guthrie Medicare Products (Melaka) Sdn Bhd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2000
Days to Decision
28 days
Submission Type
Statement