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Cope Nephroureterostomy Stent and Amplatz Ureteral Stent Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171603
510(k) Type
Traditional
Applicant
Cook Incorporated
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
4/16/2018
Days to Decision
319 days
Submission Type
Summary

Cope Nephroureterostomy Stent and Amplatz Ureteral Stent Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171603
510(k) Type
Traditional
Applicant
Cook Incorporated
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
4/16/2018
Days to Decision
319 days
Submission Type
Summary