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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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