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CONVEEN EASICATH SET

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973070
510(k) Type
Traditional
Applicant
Coloplast Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1997
Days to Decision
80 days
Submission Type
Summary

CONVEEN EASICATH SET

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973070
510(k) Type
Traditional
Applicant
Coloplast Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1997
Days to Decision
80 days
Submission Type
Summary