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SpeediCath Flex Coude Pro

Page Type
Cleared 510(K)
510(k) Number
K190620
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2019
Days to Decision
121 days
Submission Type
Summary

SpeediCath Flex Coude Pro

Page Type
Cleared 510(K)
510(k) Number
K190620
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2019
Days to Decision
121 days
Submission Type
Summary