Last synced on 14 November 2025 at 11:06 pm

Self-Cath and Self-Cath Plus

Page Type
Cleared 510(K)
510(k) Number
K221401
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2022
Days to Decision
200 days
Submission Type
Summary

Self-Cath and Self-Cath Plus

Page Type
Cleared 510(K)
510(k) Number
K221401
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2022
Days to Decision
200 days
Submission Type
Summary