510(k) K031952
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 22, 2003
- Date Received
- June 25, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Elisa, Antibody, West Nile Virus
- Device Class
- Class II
- Regulation Number
- 866.3940
- Review Panel
- MI
- Submission Type
The West Nile Virus ELISA is intended for the detection of IgG and IgM antibodies to West Nile Virus. Specimens may be serum or cerebral spinal fluid from symptomatic patients.