Last synced on 2 December 2022 at 11:04 pm

SpeedCath Compact Male

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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