Last synced on 17 May 2024 at 11:06 pm

RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232920
510(k) Type
Traditional
Applicant
Ureteral Stent Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2024
Days to Decision
185 days
Submission Type
Summary

RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232920
510(k) Type
Traditional
Applicant
Ureteral Stent Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2024
Days to Decision
185 days
Submission Type
Summary