Last synced on 20 December 2024 at 11:05 pm

RUSCH GUIDED CHOLANGIOGRAPHY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023666
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2003
Days to Decision
229 days
Submission Type
Summary

RUSCH GUIDED CHOLANGIOGRAPHY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023666
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2003
Days to Decision
229 days
Submission Type
Summary