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SELF CATH CATHETER

Page Type
Cleared 510(K)
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)
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