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Aspirex™ Thrombectomy System

Page Type
Cleared 510(K)
510(k) Number
K230356
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2023
Days to Decision
50 days
Submission Type
Summary

Aspirex™ Thrombectomy System

Page Type
Cleared 510(K)
510(k) Number
K230356
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2023
Days to Decision
50 days
Submission Type
Summary