Last synced on 15 September 2023 at 11:04 pm

Uro-N Cystoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182876
510(k) Type
Traditional
Applicant
UroViu Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2019
Days to Decision
263 days
Submission Type
Summary

Uro-N Cystoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182876
510(k) Type
Traditional
Applicant
UroViu Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2019
Days to Decision
263 days
Submission Type
Summary