Last synced on 25 January 2026 at 3:41 am

ADROIT GUIDING CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131225
510(k) Type
Special
Applicant
Cordis Corp., A Johnson & Johnson Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2013
Days to Decision
29 days
Submission Type
Summary

ADROIT GUIDING CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131225
510(k) Type
Special
Applicant
Cordis Corp., A Johnson & Johnson Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2013
Days to Decision
29 days
Submission Type
Summary