FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CEDIA (R) VITAMIN B12/FOLATE ASSAY
K Number: K904776
·
Decision Nov 20, 1990
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
107
Review Days
29
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Basic Information
- Device Name
- CEDIA (R) VITAMIN B12/FOLATE ASSAY
- K Number
- K904776
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1810
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Microgenics Corp.
- Date Received
- October 22, 1990
- Decision Date
- November 20, 1990
- 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 |
Similar 510(k) Clearances
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