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URETERAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930483
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/16/1993
Days to Decision
168 days
Submission Type
Statement

URETERAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930483
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/16/1993
Days to Decision
168 days
Submission Type
Statement