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URESIL GENERAL PURPOSE DRAINAGE CATHETER, URESIL NEPHROSTOMY CATHETER, URESIL BILIARY CATHETER, URESIL NEPHRO-URETERAL S

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972583
510(k) Type
Traditional
Applicant
Uresil Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1997
Days to Decision
50 days
Submission Type
Statement

URESIL GENERAL PURPOSE DRAINAGE CATHETER, URESIL NEPHROSTOMY CATHETER, URESIL BILIARY CATHETER, URESIL NEPHRO-URETERAL S

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972583
510(k) Type
Traditional
Applicant
Uresil Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1997
Days to Decision
50 days
Submission Type
Statement