FDA 510(k)
FDA class 2
Substantially Equivalent
🇯🇵 Japan
CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KIT
K Number: K011958
·
Decision Dec 4, 2001
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
69
Applicant Total
4
Review Days
165
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Basic Information
- Device Name
- CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KIT
- K Number
- K011958
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5270
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Denka Seiken'S
- Date Received
- June 22, 2001
- Decision Date
- December 4, 2001
- Product Code
- DCN
- 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 |
|---|---|---|---|
| DCN | System, Test, C-Reactive Protein | FDA class 2 | Immunology |
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