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ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD

Page Type
Cleared 510(K)
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)
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