FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CEDIA T4 MAB ASSAY MODIFICATION
K Number: K935880
·
Decision Mar 3, 1994
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
85
Applicant Total
107
Review Days
87
Basic Information
- Device Name
- CEDIA T4 MAB ASSAY MODIFICATION
- K Number
- K935880
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1700
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- MICROGENICS CORP.
- Date Received
- December 6, 1993
- Decision Date
- March 3, 1994
- Product Code
- KLI
- 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 |
|---|---|---|---|
| KLI | Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine | FDA class 2 | Clinical Chemistry |
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