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Flexible Sensor-Ureterorenoscopes BOA Vision EF, Flexible Sensor-Ureterorenoscopes COBRA Vision EF

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183188
510(k) Type
Traditional
Applicant
Richard Wolf Medical Instruments Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2019
Days to Decision
165 days
Submission Type
Summary

Flexible Sensor-Ureterorenoscopes BOA Vision EF, Flexible Sensor-Ureterorenoscopes COBRA Vision EF

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183188
510(k) Type
Traditional
Applicant
Richard Wolf Medical Instruments Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2019
Days to Decision
165 days
Submission Type
Summary