Last synced on 25 January 2026 at 3:41 am

SELF CATH CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100878
510(k) Type
Traditional
Applicant
Coloplast Manufacturing Us, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2010
Days to Decision
57 days
Submission Type
Summary

SELF CATH CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100878
510(k) Type
Traditional
Applicant
Coloplast Manufacturing Us, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2010
Days to Decision
57 days
Submission Type
Summary