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FLEXISKIN LATEX EXAMINATION GLOVES, POWDERED, NON STERILE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031020
510(k) Type
Traditional
Applicant
PT. MANDIRI INTI BUANA
Country
Indonesia
FDA Decision
Substantially Equivalent
Decision Date
5/21/2003
Days to Decision
51 days
Submission Type
Summary

FLEXISKIN LATEX EXAMINATION GLOVES, POWDERED, NON STERILE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031020
510(k) Type
Traditional
Applicant
PT. MANDIRI INTI BUANA
Country
Indonesia
FDA Decision
Substantially Equivalent
Decision Date
5/21/2003
Days to Decision
51 days
Submission Type
Summary