FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

Allia Moveo

K Number: K251199 · Decision Dec 9, 2025
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
37
Review Days
235

Basic Information

Device Name
Allia Moveo
K Number
K251199
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Medical Systems SCS
Date Received
April 18, 2025
Decision Date
December 9, 2025
Product Code
OWB
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
OWB Interventional Fluoroscopic X-Ray System

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