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Optilume Basic Urological Balloon Dilation Catheter

Page Type
Cleared 510(K)
510(k) Number
K191061
510(k) Type
Traditional
Applicant
Urotronic Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2020
Days to Decision
255 days
Submission Type
Summary

Optilume Basic Urological Balloon Dilation Catheter

Page Type
Cleared 510(K)
510(k) Number
K191061
510(k) Type
Traditional
Applicant
Urotronic Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2020
Days to Decision
255 days
Submission Type
Summary