Last synced on 14 November 2025 at 11:06 pm

SpeedCath Compact Male

Page Type
Cleared 510(K)
510(k) Number
K210250
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2022
Days to Decision
452 days
Submission Type
Summary

SpeedCath Compact Male

Page Type
Cleared 510(K)
510(k) Number
K210250
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2022
Days to Decision
452 days
Submission Type
Summary