Last synced on 25 January 2026 at 3:41 am

WiScope Digital Cystoscope System, WiScope Single-Use Digital Flexible Cystoscope, WiScope Image System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212202
510(k) Type
Traditional
Applicant
OTU Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2022
Days to Decision
273 days
Submission Type
Summary

WiScope Digital Cystoscope System, WiScope Single-Use Digital Flexible Cystoscope, WiScope Image System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212202
510(k) Type
Traditional
Applicant
OTU Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2022
Days to Decision
273 days
Submission Type
Summary