Last synced on 25 January 2026 at 3:41 am

RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011121
510(k) Type
Traditional
Applicant
Rusch Intl.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2001
Days to Decision
218 days
Submission Type
Summary

RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011121
510(k) Type
Traditional
Applicant
Rusch Intl.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2001
Days to Decision
218 days
Submission Type
Summary