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Dornier Ureteral Stent

Page Type
Cleared 510(K)
510(k) Number
K190312
510(k) Type
Traditional
Applicant
Dornier MedTech America Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2019
Days to Decision
276 days
Submission Type
Summary

Dornier Ureteral Stent

Page Type
Cleared 510(K)
510(k) Number
K190312
510(k) Type
Traditional
Applicant
Dornier MedTech America Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2019
Days to Decision
276 days
Submission Type
Summary