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Flexor Ureteral Access Sheath and Flexor Parallel Rapid Release Ureteral Access Sheath

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172217
510(k) Type
Traditional
Applicant
Cook Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2017
Days to Decision
142 days
Submission Type
Summary

Flexor Ureteral Access Sheath and Flexor Parallel Rapid Release Ureteral Access Sheath

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172217
510(k) Type
Traditional
Applicant
Cook Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2017
Days to Decision
142 days
Submission Type
Summary