Last synced on 14 November 2025 at 11:06 pm

SpeediCath Compact (28578, 28580, 28582, 28584), SpeediCath Compact Plus (28810, 28812, 28814)

Page Type
Cleared 510(K)
510(k) Number
K203637
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2022
Days to Decision
449 days
Submission Type
Summary

SpeediCath Compact (28578, 28580, 28582, 28584), SpeediCath Compact Plus (28810, 28812, 28814)

Page Type
Cleared 510(K)
510(k) Number
K203637
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2022
Days to Decision
449 days
Submission Type
Summary