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Aspirex Thrombectomy System

Page Type
Cleared 510(K)
510(k) Number
K220270
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2022
Days to Decision
141 days
Submission Type
Summary

Aspirex Thrombectomy System

Page Type
Cleared 510(K)
510(k) Number
K220270
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2022
Days to Decision
141 days
Submission Type
Summary