510(k) K253584

Device
Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve Imaging (FOV Extension)
Applicant
Canon Medical Systems Corporation
510(k) number
K253584
Product code
OWB
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-10
Date received
2025-11-17
Regulation
892.1650
Classification name
Interventional Fluoroscopic X-Ray System
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Orlando Tadeo, Jr.
Address
1385 Shimoishigami Otawara-Shi JP 324-8550 324-8550

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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