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Uro-V Cystoscope

Page Type
Cleared 510(K)
510(k) Number
K171500
510(k) Type
Traditional
Applicant
UroViu Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2018
Days to Decision
252 days
Submission Type
Summary

Uro-V Cystoscope

Page Type
Cleared 510(K)
510(k) Number
K171500
510(k) Type
Traditional
Applicant
UroViu Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2018
Days to Decision
252 days
Submission Type
Summary