FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
Lp(a) Ultra
K Number: K211058
·
Decision Dec 22, 2022
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
42
Applicant Total
12
Review Days
622
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Basic Information
- Device Name
- Lp(a) Ultra
- K Number
- K211058
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5600
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- SENTINEL CH. SpA
- Date Received
- April 9, 2021
- Decision Date
- December 22, 2022
- Product Code
- DFC
- 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 |
|---|---|---|---|
| DFC | Lipoprotein, Low-Density, Antigen, Antiserum, Control | FDA class 2 | Immunology |
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