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MODIFICATION TO: ULTRALON (R) POWDER FREE LATEX SURGICAL GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013604
510(k) Type
Special
Applicant
ANSELL HEALTHCARE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2001
Days to Decision
13 days
Submission Type
Summary

MODIFICATION TO: ULTRALON (R) POWDER FREE LATEX SURGICAL GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013604
510(k) Type
Special
Applicant
ANSELL HEALTHCARE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2001
Days to Decision
13 days
Submission Type
Summary