510(k) · Cleared

Cleared

Q Fever Igm Ifa Test

K922374510(k) TraditionalCleared Oct 21, 1992154-day reviewClass I21 CFR 866.3500

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

Hillcrest Biologicals · GPJ Antiserum, Fluorescent, Q Fever

Cleared on Oct 21, 1992 after a 154-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided: Oct 21, 1992
Review: 154 days
Class: Class I
Product code: GPJ
Recalls: None
Predicates: 0

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

This deviceK922374 Q Fever Igm Ifa TestHillcrest Biologicals · 1992
Descendant · cites it directly · 0 of its ownK103207 Jbaids Q Fever Detection KitIdaho Technology, Inc. · 2011

Most influential descendants

Showing 1 of 1 · See all

K103207Jbaids Q Fever Detection KitIdaho Technology, Inc. · 2011 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K922374	Q Fever Igm Ifa Test	Hillcrest Biologicals	1992	—
+1	K103207	Jbaids Q Fever Detection Kit	Idaho Technology, Inc.	2011	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2011	1	0

FIG. 1 — Lineage of K922374, 1992–2011Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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

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Candidate predicates for a device like this, rankedin the report
Recall history across each candidate’s familyin the report

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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (1)

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

Number	Device	Applicant	Decided	Descendants
K103207	Jbaids Q Fever Detection Kit	Idaho Technology, Inc.	2011	0

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, K103207 (Idaho Technology, Inc., 2011) has gone furthest, with 0 descendants of its own.

How does its category compare?

All GPJ devices

GPJ Antiserum, Fluorescent, Q Fever: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GPJ

FDA has decided no GPJ device since 2007.

Median 510(k) review, days · GPJ

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

Recalls per year · GPJ

No recall names GPJ since 2007.

Adverse event reports per year · GPJ

No MAUDE report names GPJ since 2007.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	0
2011	—	0
2012	—	0
2013	—	0
2014	—	0
2015	—	0
2016	—	0
2017	—	0
2018	—	0
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

https://510kreport.com/device/K922374 · printed Nov 6, 2026

Cite this page

510(k) Report. “K922374: Q Fever Igm Ifa Test.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K922374

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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