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GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
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)
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