510(k) Report

De Novo · Granted

Granted

West Nile Virus Igm Capture Elisa

DEN030004De NovoGranted Jul 8, 20035-day reviewClass II21 CFR 866.3940

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Panbio Limited · NOP Elisa, Antibody, West Nile Virus

Granted on Jul 8, 2003 as a new device type through De Novo after a 5-day review. 1 later device descends from it.

Decided
Jul 8, 2003
Review
5 days
Class
Class II
Product code
NOP
Recalls
None

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared200020052010201520202025
  1. This deviceDEN030004 West Nile Virus Igm Capture ElisaPanbio Limited · 2003
  2. Descendant · cites it directly · 0 of its ownK041231 West Nile Virus Igm Capture Elisa, Model E-WNV02MPanbio Limited · 2004 · Recalled

Most influential descendants

Showing 1 of 1 · See all
  • K041231West Nile Virus Igm Capture Elisa, Model E-WNV02MPanbio Limited · 2004 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)DEN030004West Nile Virus Igm Capture ElisaPanbio Limited2003—
+1K041231West Nile Virus Igm Capture Elisa, Model E-WNV02MPanbio Limited20041

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
FIG. 1 — Lineage of DEN030004, 2003–2004Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA De Novo database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in NOP? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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Does it have a predicate?

De Novo decisions do not claim a predicate device.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K041231West Nile Virus Igm Capture Elisa, Model E-WNV02MPanbio Limited20040

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K041231 (Panbio Limited, 2004) has gone furthest, with 0 descendants of its own.

How does its category compare?

All NOP devices

NOP Elisa, Antibody, West Nile Virus: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · NOP

2in 2016

2016: 2
2007high 2 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NOP

Too few NOP 510(k)s in any year since 2007 to give a median.

Recalls per year · NOP

1in 2012

2008: 12012: 1
2007high 1 (2008) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · NOP

1in 2019

2007: 12013: 12014: 12019: 1
2007high 1 (2007) · low 0 (2008)2025

MAUDE reports naming product code NOP, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—01
20080—10
20090—00
20100—00
20110—00
20120—10
20130—01
20140—01
20150—00
20162—00
20170—00
20180—00
20190—01
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “DEN030004: West Nile Virus Igm Capture Elisa.” Lineage record from FDA De Novo data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/DEN030004

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026