Last synced on 18 April 2025 at 11:05 pm

VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System

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