FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
InferRead Lung CT.AI
K Number: K240554
·
Decision May 16, 2025
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
19
Applicant Total
2
Review Days
443
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Basic Information
- Device Name
- InferRead Lung CT.AI
- K Number
- K240554
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Infervision Medical Technology Co., Ltd.
- Date Received
- February 28, 2024
- Decision Date
- May 16, 2025
- Product Code
- OEB
- 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 |
|---|---|---|---|
| OEB | Lung Computed Tomography System, Computer-Aided Detection | FDA class 2 | Radiology |
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Other Clearances by Infervision Medical Technology Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K211179 | InferRead CT Stroke.AI | Aug 12, 2021 | Substantially Equivalent |