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CROSSER CTO Recanalization Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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