Last synced on 14 November 2025 at 11:06 pm

Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter

Page Type
Cleared 510(K)
510(k) Number
K210655
510(k) Type
Traditional
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2022
Days to Decision
447 days
Submission Type
Summary

Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter

Page Type
Cleared 510(K)
510(k) Number
K210655
510(k) Type
Traditional
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2022
Days to Decision
447 days
Submission Type
Summary