Last synced on 20 December 2024 at 11:05 pm

Uretero1 Single-Use Digital Flexible Ureteroscope (standard deflection), PN UROSD101, Uretero1 Single-Use Digital Flexible Ureteroscope (reverse deflection), PN URORD101, Vision1 Imaging Console and Display System, PN VIS101

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231878
510(k) Type
Special
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2023
Days to Decision
29 days
Submission Type
Summary

Uretero1 Single-Use Digital Flexible Ureteroscope (standard deflection), PN UROSD101, Uretero1 Single-Use Digital Flexible Ureteroscope (reverse deflection), PN URORD101, Vision1 Imaging Console and Display System, PN VIS101

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231878
510(k) Type
Special
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2023
Days to Decision
29 days
Submission Type
Summary