Last synced on 30 May 2025 at 11:05 pm

LumiRex Ureteroscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243532
510(k) Type
Traditional
Applicant
Contra Healthcare Solutions, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2025
Days to Decision
164 days
Submission Type
Summary

LumiRex Ureteroscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243532
510(k) Type
Traditional
Applicant
Contra Healthcare Solutions, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2025
Days to Decision
164 days
Submission Type
Summary