Last synced on 14 November 2025 at 11:06 pm

WiScope® Digital Cystoscope System, WiScope® Single-Use Digital Flexible Cystoscope, WiScope® Medical Tablet

Page Type
Cleared 510(K)
510(k) Number
K231702
510(k) Type
Traditional
Applicant
OTU Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2023
Days to Decision
109 days
Submission Type
Summary

WiScope® Digital Cystoscope System, WiScope® Single-Use Digital Flexible Cystoscope, WiScope® Medical Tablet

Page Type
Cleared 510(K)
510(k) Number
K231702
510(k) Type
Traditional
Applicant
OTU Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2023
Days to Decision
109 days
Submission Type
Summary