FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
EQ-PRC LC WARFARIN GENOTYPING KIT
K Number: K073071
·
Decision Feb 6, 2009
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
5
Applicant Total
1
Review Days
464
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Basic Information
- Device Name
- EQ-PRC LC WARFARIN GENOTYPING KIT
- K Number
- K073071
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3360
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Trimgen Corporation
- Date Received
- October 31, 2007
- Decision Date
- February 6, 2009
- Product Code
- ODW
- 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 |
|---|---|---|---|
| ODW | Cytochrome P450 2c9 (Cyp450 2c9) Drug Metabolizing Enzyme Genotyping System | FDA class 2 | Clinical Toxicology |
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