Last synced on 25 January 2026 at 3:41 am

REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160583
510(k) Type
Traditional
Applicant
Volcano Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2016
Days to Decision
239 days
Submission Type
Summary

REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160583
510(k) Type
Traditional
Applicant
Volcano Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2016
Days to Decision
239 days
Submission Type
Summary