FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
InferRead Lung CT.AI
K Number: K192880
·
Decision Jul 2, 2020
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
19
Applicant Total
1
Review Days
267
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Basic Information
- Device Name
- InferRead Lung CT.AI
- K Number
- K192880
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Beijing Infervision Technology Co., Ltd.
- Date Received
- October 9, 2019
- Decision Date
- July 2, 2020
- 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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