Atlas FDA

WEST NILE VIRUS IGM CAPTURE ELISA

FDA 510(k) clearance K040854 · decided 2004-06-30

Clearance details

K-number
K040854
Device name
WEST NILE VIRUS IGM CAPTURE ELISA
Applicant
Focus Technologies, Inc.
Decision
Substantially Equivalent
Date received
2004-04-01
Decision date
2004-06-30
Days to decision
90 days
Clearance type
Traditional
Product code
NOP
Device class
2
Regulation number
866.3940
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Cypress, CA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Focus Technologies

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
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 Limited2004-10-20
WEST NILE VIRUS IGM CAPTURE ELISA, MODEL E-WNV02M (K041231)Panbio Limited2004-08-10
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
WEST NILE VIRUS IGM CAPTURE ELISA (DEN030004)Panbio Limited2003-07-08

Recalls involving this device

No recalls on record reference this clearance.