West Nile Virus Igg Indirect Elisa

FDA 510(k) K041068 · Panbio Limited

Substantially Equivalent

510(k) numberK041068

Submission

Device name
West Nile Virus Igg Indirect Elisa
Applicant
Panbio Limited
Windsor, AU
Received
April 26, 2004
Decision date
October 20, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NOP – Elisa, Antibody, West Nile Virus
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3940
Specialty
Microbiology

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.

Other 510(k)s with product code NOP

510(k)DeviceApplicantDecision
K153308EUROIMMUN Anti-West Nile Virus ELISA (IgM)NOP · Traditional Euroimmun Us, Inc.08/12/2016SE
K153303EUROIMMUN Anti-West Nile Virus ELISA (IgG)NOP · Traditional Euroimmun Us, Inc.08/10/2016SE
K052519Spectral West Nile Virus Igm Status TestNOP · Traditional Spectral Diagnostics, Inc.11/30/2006SE
K041817West Nile Detect Igm ElisaNOP · Traditional Inbios Intl., Inc.11/19/2004SE
K041231West Nile Virus Igm Capture Elisa, Model E-WNV02MNOP · Traditional Panbio Limited08/10/2004SE
K040854West Nile Virus Igm Capture ElisaNOP · Traditional Focus Technologies, Inc.06/30/2004SE
K031953West Nile Virus Elisa Igg, Model EL0300GNOP · Traditional Focus Technologies, Inc.10/22/2003SE
K031952West Nile Virus Igm Capture Elisa, Model EL0300MNOP · Traditional Focus Technologies, Inc.10/22/2003SE

More from Focus Technologies, Inc.

510(k)DeviceDecision
K041231West Nile Virus Igm Capture Elisa, Model E-WNV02MNOP · Traditional 08/10/2004SE
K030863Ebv VCA-P18 Igg ElisaLSE · Traditional 06/27/2003SE
K002024Panbio Indx Igm Dip-S-Ticks Leptospirosis Test for the Detection of Igm Antibodies to…GRY · Traditional 11/22/2000SE
K970189Fif TMKQJ · Traditional 05/21/1997SE
K962176TPPMIF · Traditional 10/18/1996SE
K910636Abs CadkitGIS · Traditional 04/29/1991SE

Questions and answers

When was West Nile Virus Igg Indirect Elisa cleared by the FDA?

West Nile Virus Igg Indirect Elisa (K041068) received a 510(k) decision of Substantially Equivalent on October 20, 2004, 177 days after the submission was received.

What is the product code of K041068?

The FDA product code is NOP – Elisa, Antibody, West Nile Virus, a Class II (moderate risk) device regulated under 21 CFR 866.3940.