FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
EMIT II PLUS MONOCLONAL COCAINE METABOLITE ASSAY
K Number: K020441
·
Decision Mar 28, 2002
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
343
Review Days
45
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Basic Information
- Device Name
- EMIT II PLUS MONOCLONAL COCAINE METABOLITE ASSAY
- K Number
- K020441
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3250
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Dade Behring, Inc.
- Date Received
- February 11, 2002
- Decision Date
- March 28, 2002
- Product Code
- DIO
- Advisory Committee
- Clinical Toxicology
- Review Advisory Committee
- TX
- 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 |
|---|---|---|---|
| DIO | Enzyme Immunoassay, Cocaine And Cocaine Metabolites | FDA class 2 | Clinical Toxicology |
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Carolina Liquid Chemistries Cocaine and Cocaine Metabolite Test System (COCM)
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