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

BELLIGER ACE

K Number: K252229 · Decision Apr 2, 2026
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
24
Review Days
260

Basic Information

Device Name
BELLIGER ACE
K Number
K252229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genoray Co., Ltd.
Date Received
July 16, 2025
Decision Date
April 2, 2026
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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