Last synced on 2 December 2022 at 11:04 pm

SpeediCath Flex Coude Pro

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180070
510(k) Type
Special
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2018
Days to Decision
24 days
Submission Type
Summary

SpeediCath Flex Coude Pro

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180070
510(k) Type
Special
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2018
Days to Decision
24 days
Submission Type
Summary