Last synced on 14 November 2025 at 11:06 pm

VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System

Page Type
Cleared 510(K)
510(k) Number
K242893
510(k) Type
Traditional
Applicant
Luma Vision Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
3/24/2025
Days to Decision
182 days
Submission Type
Summary

VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System

Page Type
Cleared 510(K)
510(k) Number
K242893
510(k) Type
Traditional
Applicant
Luma Vision Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
3/24/2025
Days to Decision
182 days
Submission Type
Summary