510(k) Report

510(k) · Cleared

Cleared

Reaads Iga Anti-B2GP 1 Test Kit

K982434510(k) TraditionalCleared Dec 22, 1998161-day reviewClass II21 CFR 866.5660

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

Corgenix, Inc. · MSV System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi)

Cleared on Dec 22, 1998 as substantially equivalent to K973006 (Inova Diagnostics, Inc., 1997) after a 161-day review. Its family tree reaches back 1 generation to 1997.

Decided
Dec 22, 1998
Review
161 days
Class
Class II
Product code
MSV
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K973006 (1997). No later device cites it as a predicate yet.

K973006 · Quanta Lite B2 Gpi Iga · Inova Diagnostics, Inc. · 1997199619982000
K973006 · Quanta Lite B2 Gpi Iga · Inova Diagnostics, Inc. · 19970
  1. Root · 1 generation backK973006 Quanta Lite B2 Gpi IgaInova Diagnostics, Inc. · 1997
  2. This deviceK982434 Reaads Iga Anti-B2GP 1 Test KitCorgenix, Inc. · 1998
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K973006Quanta Lite B2 Gpi IgaInova Diagnostics, Inc.1997—
0 (this device)K982434Reaads Iga Anti-B2GP 1 Test KitCorgenix, Inc.1998—
FIG. 1 — Lineage of K982434, 1997–1998Source: 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 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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

Top candidate predicates for a new MSV device

  1. #1 K243979 Aptiva APS IgA Reagentscore 10.8 · 1 generation · no Class I recall
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K973006Quanta Lite B2 Gpi Iga
Summary page 1
…nti-B2GPI Test Kit is compared to a legally marketed predicate device and a substantial equivalence claim made. The predicate device is QUANTA Lite IgA anti B2GPI ELISA (K973006) currently manufactured and marketed by INOVA Diagnostics, Inc., San Diego, California. The REAADS IgA anti-B2GPI Test Kit is an…
Inova Diagnostics, Inc.1997—

What descends from it?

No later submission names this one as a predicate yet.

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?

  • Its one ancestor has no recall.

How does its category compare?

All MSV devices

MSV System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MSV

1in 2018

2008: 12009: 12010: 12012: 12015: 22017: 12018: 12026 (partial year): 1
2007high 2 (2015) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSV

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

Recalls per year · MSV

No recall names MSV since 2007.

Adverse event reports per year · MSV

No MAUDE report names MSV since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20081—00
20091—00
20101—00
20110—00
20121—00
20130—00
20140—00
20152—00
20160—00
20171—00
20181—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20261—0—

What is it indicated for?

The REAADS IgA anti-B2GPI Test Kit is an in vitro diagnostic assay for the detection and semi-quantitation of IgA anti-B2GPI antibodies in human serum as an aid for assessing the risk of thrombosis in individuals with

systemic lupus erythematosus (SLE) and lupus-like disorders (antiphospholipid syndrome).

The REAADS IgA anti-B2GPI Test Kit is intended to be used by clinical (hospital and reference) laboratories.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K982434: Reaads Iga Anti-B2GP 1 Test Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K982434

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026