FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
CRP Vario
K Number: K173833
·
Decision Sep 27, 2018
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
18
Applicant Total
12
Review Days
283
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Basic Information
- Device Name
- CRP Vario
- K Number
- K173833
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5270
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- SENTINEL CH. SpA
- Date Received
- December 18, 2017
- Decision Date
- September 27, 2018
- Product Code
- NQD
- Advisory Committee
- Immunology
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| NQD | Cardiac C-Reactive Protein, Antigen, Antiserum, And Control | FDA class 2 | Immunology |
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