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Uretero1 Ureteroscope System

Page Type
Cleared 510(K)
510(k) Number
K211347
510(k) Type
Traditional
Applicant
Steris Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2021
Days to Decision
204 days
Submission Type
Summary

Uretero1 Ureteroscope System

Page Type
Cleared 510(K)
510(k) Number
K211347
510(k) Type
Traditional
Applicant
Steris Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2021
Days to Decision
204 days
Submission Type
Summary