Last synced on 14 November 2025 at 11:06 pm

SpeediCath Flex Set

Page Type
Cleared 510(K)
510(k) Number
K222059
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2022
Days to Decision
70 days
Submission Type
Summary

SpeediCath Flex Set

Page Type
Cleared 510(K)
510(k) Number
K222059
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2022
Days to Decision
70 days
Submission Type
Summary