FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6
K Number: K060929
·
Decision Apr 28, 2006
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
3
Review Days
23
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Basic Information
- Device Name
- IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6
- K Number
- K060929
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 862.1810
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Diagnostic Products Corporation
- Date Received
- April 5, 2006
- Decision Date
- April 28, 2006
- Product Code
- CDD
- Advisory Committee
- Clinical Chemistry
- 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 |
|---|---|---|---|
| CDD | Radioassay, Vitamin B12 | FDA class 2 | Clinical Chemistry |
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