FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

OEC One CFD

K Number: K253269 · Decision Nov 26, 2025
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
81
Applicant Total
12
Review Days
58

Basic Information

Device Name
OEC One CFD
K Number
K253269
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Hualun Medical Systems Co. , Ltd.
Date Received
September 29, 2025
Decision Date
November 26, 2025
Product Code
OXO
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
OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

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K172700 OEC One
K172869 Discovery XR656 HD
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