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 | Device Class | Medical Specialty |
|---|---|---|---|
| OWB | Interventional Fluoroscopic X-Ray System | FDA class 2 | Radiology |
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