FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
CRP Vario
K Number: K192118
·
Decision Nov 8, 2019
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
12
Review Days
94
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Basic Information
- Device Name
- CRP Vario
- K Number
- K192118
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 866.5270
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- SENTINEL CH. SpA
- Date Received
- August 6, 2019
- Decision Date
- November 8, 2019
- Product Code
- DCK
- Advisory Committee
- Immunology
- Review Advisory Committee
- IM
- 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 |
|---|---|---|---|
| DCK | C-Reactive Protein, Antigen, Antiserum, And Control | FDA class 2 | Immunology |
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