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URETERAL STENT

Page Type
Cleared 510(K)
510(k) Number
K930733
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1993
Days to Decision
162 days
Submission Type
Statement

URETERAL STENT

Page Type
Cleared 510(K)
510(k) Number
K930733
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1993
Days to Decision
162 days
Submission Type
Statement