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PolarCath Peripheral Dilatation System

Page Type
Cleared 510(K)
510(k) Number
K152665
510(k) Type
Traditional
Applicant
NUCYRO VASCULAR, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2015
Days to Decision
39 days
Submission Type
Summary

PolarCath Peripheral Dilatation System

Page Type
Cleared 510(K)
510(k) Number
K152665
510(k) Type
Traditional
Applicant
NUCYRO VASCULAR, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2015
Days to Decision
39 days
Submission Type
Summary