FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Synapse 3D Base Tools (V7.2)

K Number: K254189 · Decision Apr 30, 2026
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
303
Applicant Total
64
Review Days
128

Basic Information

Device Name
Synapse 3D Base Tools (V7.2)
K Number
K254189
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fujifilm Corporation
Date Received
December 23, 2025
Decision Date
April 30, 2026
Product Code
QIH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QIH Automated Radiological Image Processing Software

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