FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Cornaris Intravascular Imaging System (P80-E); Cornaris Intravascular Imaging System (Mobile-E); LumenCross Imaging Catheter (F2)
K Number: K242098
·
Decision Apr 11, 2025
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
45
Applicant Total
1
Review Days
267
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Basic Information
- Device Name
- Cornaris Intravascular Imaging System (P80-E); Cornaris Intravascular Imaging System (Mobile-E); LumenCross Imaging Catheter (F2)
- K Number
- K242098
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1560
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Shenzhen Vivolight Medical Device & Technology Co., Ltd.
- Date Received
- July 18, 2024
- Decision Date
- April 11, 2025
- Product Code
- NQQ
- Advisory Committee
- Radiology
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| NQQ | System, Imaging, Optical Coherence Tomography (Oct) | FDA class 2 | Radiology |
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