Last synced on 25 April 2025 at 11:05 pm

ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011056
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2001
Days to Decision
201 days
Submission Type
Summary

ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011056
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2001
Days to Decision
201 days
Submission Type
Summary