510(k) K242893

Device
VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System
Applicant
Luma Vision Limited
510(k) number
K242893
Product code
OBJ
Decision
Substantially Equivalent (SESE)
Decision date
2025-03-24
Date received
2024-09-23
Regulation
870.1200
Classification name
Catheter, Ultrasound, Intravascular
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Marta Walker
Address
Block C, Parkview House-Beech Hill Office Campus Beech Hill Rd. Dublin IE D04 K5D0 D04 K5D0

FDA Registration Numbers

Source Documents

510(k) summary PDF

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