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CROSSER CTO Recanalization Catheter

Page Type
Cleared 510(K)
510(k) Number
K161208
510(k) Type
Special
Applicant
Bard Peripheral Vacular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2016
Days to Decision
26 days
Submission Type
Summary

CROSSER CTO Recanalization Catheter

Page Type
Cleared 510(K)
510(k) Number
K161208
510(k) Type
Special
Applicant
Bard Peripheral Vacular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2016
Days to Decision
26 days
Submission Type
Summary