510(k) Report

510(k) · Cleared

Cleared

Xpert Flu

K123191510(k) TraditionalCleared Dec 21, 201271-day reviewClass II21 CFR 866.3980

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

Cepheid · OCC Respiratory Virus Panel Nucleic Acid Assay System

Cleared on Dec 21, 2012 as substantially equivalent to K120911 (Cepheid, 2012) after a 71-day review. Its family tree reaches back 6 generations to 2008. 6 later devices descend from it.

Decided
Dec 21, 2012
Review
71 days
Class
Class II
Product code
OCC
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to DEN070013 (2008). 9 ancestors in all, the oldest DEN060008 (2006). 6 later devices descend from it, 1 citing it directly.

  1. Root · 6 generations backDEN070013 ID-Tag Respiratory Viral PanelLuminex Molecular Diagnostics, Inc. · 2008
  2. 5 generations backK081483 Xtag Respiratory Viral PanelLuminex Molecular Diagnostics, Inc. · 2008 · Recalled
  3. 4 generations backK091667 Xtag Respiratory Viral Panel, Models I019A0110, I019C011, I019D0112…Luminex Molecular Diagnostics, Inc. · 2009 · Recalled
  4. 3 generations backK100148 Simplexa Influenza a H1N1 (2009) Model MOL2500Focus Diagnostics, Inc. · 2010
  5. 2 generations backK103766 Xpert Flu, Genexpert DX Systems, Genexpert Infinity System…Cepheid · 2011 · Recalled
  6. 1 generation backK120911 Xpert Flu Genexpert DX Systems (GX-I, GX-IV)Cepheid · 2012
  7. This deviceK123191 Xpert FluCepheid · 2012
  8. Descendant · cites it directly · 5 of its ownK142045 Xpert Flu/RSV XC AssayCepheid · 2014
  9. Descendant · 2 generations on · 4 of its ownK151226 Xpert Flu+RSV Xpress, Xpert Nasopharyngeal Sample Collection Kit…Cepheid · 2015
  10. Descendant · 2 generations on · 2 of its ownK162456 Xpert Xpress Flu, Xpert Nasopharyngeal Sample Collection Kit…Cepheid · 2017
  11. Descendant · 3 generations on · 1 of its ownK171552 Xpert Xpress Flu, Xpert Nasopharyngeal Sample Collection Kit, Xpert…Cepheid · 2017
  12. Descendant · 3 generations on · 0 of its ownK180218 Xpert Xpress Flu/RSV, Xpert Nasopharyngeal Sample Collection Kit…Cepheid · 2018

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2014: 12015: 12017: 32018: 1
2014high 3 (2017) · low 0 (2016)2026

Most influential descendants

Showing 5 of 6 · See all
  • K142045Xpert Flu/RSV XC AssayCepheid · 2014 · cites it directly5descendants
  • K151226Xpert Flu+RSV Xpress, Xpert Nasopharyngeal Sample Collection Kit, GeneXpert Xpress…Cepheid · 2015 · 2 generations on4descendants
  • K162456Xpert Xpress Flu, Xpert Nasopharyngeal Sample Collection Kit, GeneXpert Dx Systems…Cepheid · 2017 · 2 generations on2descendants
  • K171552Xpert Xpress Flu, Xpert Nasopharyngeal Sample Collection Kit, Xpert Nasal Sample…Cepheid · 2017 · 3 generations on1descendant
  • K180218Xpert Xpress Flu/RSV, Xpert Nasopharyngeal Sample Collection Kit, Xpert Nasal Sample…Cepheid · 2018 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6DEN070013ID-Tag Respiratory Viral PanelLuminex Molecular Diagnostics, Inc.2008—
−5K081483Xtag Respiratory Viral PanelLuminex Molecular Diagnostics, Inc.20081
−4K091667Xtag Respiratory Viral Panel, Models I019A0110, I019C011, I019D0112…Luminex Molecular Diagnostics, Inc.20091
−3K100148Simplexa Influenza a H1N1 (2009) Model MOL2500Focus Diagnostics, Inc.2010—
−2K103766Xpert Flu, Genexpert DX Systems, Genexpert Infinity System, Genexpert System…Cepheid20111
−1K120911Xpert Flu Genexpert DX Systems (GX-I, GX-IV)Cepheid2012—
0 (this device)K123191Xpert FluCepheid2012—
+1K142045Xpert Flu/RSV XC AssayCepheid2014—
+2K151226Xpert Flu+RSV Xpress, Xpert Nasopharyngeal Sample Collection Kit, GeneXpert…Cepheid2015—
+2K162456Xpert Xpress Flu, Xpert Nasopharyngeal Sample Collection Kit, GeneXpert Dx…Cepheid2017—
+3K171552Xpert Xpress Flu, Xpert Nasopharyngeal Sample Collection Kit, Xpert Nasal…Cepheid2017—
+3K180218Xpert Xpress Flu/RSV, Xpert Nasopharyngeal Sample Collection Kit, Xpert Nasal…Cepheid2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200610
200820

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201510
201730
201810
FIG. 1 — Lineage of K123191, 2008–2018Source: 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 OCC? 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 OCC device

  1. #1 K262747 ID NOW Influenza A & B 2; ID NOW RSV; ID NOW…score 15.2 · 12 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K120911Xpert Flu Genexpert DX Systems (GX-I, GX-IV)
Summary page 1
…y Product code: OQW, 0CC, 001 Classification Microbiology (83) Advisory Panel Predicate Device: Cepheid Xpert Flu Assay [5 10(k) #K1 20911I Device Description: The Xpert Flu Assay is a rapid, automated in vitro diagnostic test for qualitative detection and differen…
Cepheid2012—
†K103766Xpert Flu, Genexpert DX Systems, Genexpert Infinity System, Genexpert System Software…Cepheid20111

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K142045Xpert Flu/RSV XC AssayCepheid20145

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?

  • The line of descent spans 4 years and passes through 3 companies; a new generation was cleared every 11 months on median.
  • 3 of the 9 ancestors have a recall of any class.
  • Of its descendants, K142045 (Cepheid, 2014) has gone furthest, with 5 descendants of its own.

How does its category compare?

All OCC devices

OCC Respiratory Virus Panel Nucleic Acid Assay System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · OCC

1in 2024

2008: 42009: 62010: 22011: 92012: 62013: 62014: 42015: 82016: 72017: 102018: 42019: 52020: 22021: 12022: 12023: 22024: 12026 (partial year): 3
2007high 10 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OCC

31in 2019

2008: 28 days median2009: 24 days median2011: 82 days median2012: 125 days median2013: 79 days median2014: 94 days median2015: 85 days median2016: 92 days median2017: 136 days median2018: 134 days median2019: 31 days median2026 (partial year): 130 days median
2007high 136 (2017) · low 24 (2009)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · OCC

1in 2024

2014: 12018: 12019: 12024: 1
2007high 1 (2014) · low 0 (2007)2026

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

Adverse event reports per year · OCC

2in 2025

2011: 22012: 12014: 522015: 12016: 362017: 12018: 12019: 22020: 172021: 6862022: 22023: 12024: 32025: 2
2007high 686 (2021) · low 0 (2007)2025

MAUDE reports naming product code OCC, 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—00
200842800
200962400
20102—00
201198202
2012612501
201367900
2014494152
201588501
2016792036
20171013601
2018413411
201953112
20202—017
20211—0686
20221—02
20232—01
20241—13
20250—02
202631300—

What is it indicated for?

The Cepheid Xpert®o Flu Assay, performed on the GeneXpert® Instrument Systems, is an automated, multiplex real-time RT-PCR assay intended for the in vitro qualitative detection and differentiation of influenza A, influenza B and 2009 HLNI influenza viral RNA. The Xpert Flu Assay uses nasal aspirates/washes and nasopharyngeal swab* specimens collected from patients with signs and symptoms of respiratory infection in conjunction with clinical and…

Read the full statement (234 words)

The Cepheid Xpert®o Flu Assay, performed on the GeneXpert® Instrument Systems, is an automated, multiplex real-time RT-PCR assay intended for the in vitro qualitative detection and differentiation of influenza A, influenza B and 2009 HLNI influenza viral RNA. The Xpert Flu Assay uses nasal aspirates/washes and nasopharyngeal swab* specimens collected from patients with signs and symptoms of respiratory infection in conjunction with clinical and epidemiological risk factors. The Xpert Flu Assay is intended as an aid in the diagnosis of influenza.

Negative results do not preclude influenza virus infection and should not be used as the sole basis for treatment or other patient management decisions.

Performance characteristics for influenza A were established during the 2009-2010 influenza season when 2009 HiNL influenza was the predominant influenza A virus in circulation. Performance characteristics for influenza A were confirmed when influenza A/H3 and influenza A/2009 HIM were the predominant influenza A viruses in circulation (2009-2010, 2010-2011 and 2011-2012). When other influenza A viruses are emerging, performance characteristics may vary.

If infection with a novel influenza A virus is suspected based on current clinical and epidemiological screening criteria recommended by public health authorities, specimens should be collected with appropriate infection control precautions for novel virulent influenza viruses and sent to state or local health department for testing. Viral culture should not be attempted in these cases unless a BSL 3+ facility is available to receive and culture specimens.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K123191: Xpert Flu.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123191

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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