Last synced on 9 December 2022 at 11:04 pm

Ureteral Dilator Sets, Ureteral Dilators

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173654
510(k) Type
Traditional
Applicant
Cook Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2018
Days to Decision
231 days
Submission Type
Summary

Ureteral Dilator Sets, Ureteral Dilators

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173654
510(k) Type
Traditional
Applicant
Cook Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2018
Days to Decision
231 days
Submission Type
Summary