WEST NILE VIRUS IGM CAPTURE ELISA
FDA 510(k) clearance DEN030004 · decided 2003-07-08
Clearance details
- K-number
- DEN030004
- Device name
- WEST NILE VIRUS IGM CAPTURE ELISA
- Applicant
- Panbio Limited
- Decision
- Unknown
- Date received
- 2003-07-03
- Decision date
- 2003-07-08
- Days to decision
- 5 days
- Clearance type
- Post-NSE
- Product code
- NOP
- Device class
- 2
- Regulation number
- 866.3940
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Windsor, AU
- Third-party review
- No
- Expedited review
- No
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| Record | Firm | Date |
|---|---|---|
| EUROIMMUN Anti-West Nile Virus ELISA (IgM) (K153308) | Euroimmun Us, Inc. | 2016-08-12 |
| EUROIMMUN Anti-West Nile Virus ELISA (IgG) (K153303) | Euroimmun Us, Inc. | 2016-08-10 |
| SPECTRAL WEST NILE VIRUS IGM STATUS TEST (K052519) | Spectral Diagnostics, Inc. | 2006-11-30 |
| WEST NILE DETECT IGM ELISA (K041817) | Inbios Intl., Inc. | 2004-11-19 |
| WEST NILE VIRUS IGG INDIRECT ELISA (K041068) | Panbio Limited | 2004-10-20 |
| WEST NILE VIRUS IGM CAPTURE ELISA, MODEL E-WNV02M (K041231) | Panbio Limited | 2004-08-10 |
| WEST NILE VIRUS IGM CAPTURE ELISA (K040854) | Focus Technologies, Inc. | 2004-06-30 |
| WEST NILE VIRUS IGM CAPTURE ELISA, MODEL EL0300M (K031952) | Focus Technologies, Inc. | 2003-10-22 |
| WEST NILE VIRUS ELISA IGG, MODEL EL0300G (K031953) | Focus Technologies, Inc. | 2003-10-22 |
Recalls involving this device
No recalls on record reference this clearance.