510(k) · Cleared
ClearedBD Veritor System for the Rapid Detection of Flu a+B
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Becton, Dickinson and Company · PSZ Devices Detecting Influenza A, B, And C Virus Antigens
Cleared on Sep 23, 2013 as substantially equivalent to K112277 (Becton, Dickinson and Company, 2011) and 1 other predicate after a 25-day review. Its family tree reaches back 8 generations to 1990. 17 later devices descend from it.
- Decided
- Sep 23, 2013
- Review
- 25 days
- Class
- Class II
- Product code
- PSZ
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 8 generations to K902609 (1990). 10 ancestors in all. 17 later devices descend from it, 7 citing it directly.
- Root · 8 generations backK902609 Directigen Flu aBd Becton Dickinson Vacutainer Systems Preanalytic · 1990
- 7 generations backK981651 AB Flu OiaBiostar, Inc. · 1998
- 6 generations backK023556 Flu Oia a/B Test KitThermo Biostar, Inc. · 2003 · Recalled
- 5 generations backK031899 Quickvue Influenza a+B TestQuidel Corp. · 2003
- 4 generations backK053146 Quickvue Influenza a + B TestQuidel Corp. · 2005
- 3 generations backK092698 Quickvue Influenza a+B TestQuidel Corp. · 2009
- 2 generations backK112277 BD Veritor (TM) System for Rapid Detection of Flu a+BBecton, Dickinson and Company · 2011 · Recalled
- 1 generation backK132259 BD Veritor System for the Rapid Detection of Flu a+BBecton, Dickinson and Company · 2013
- This deviceK132692 BD Veritor System for the Rapid Detection of Flu a+BBecton, Dickinson and Company · 2013
- Descendant · cites it directly · 11 of its ownK151291 BD Veritor (TM) System for the Rapid Detection of Flu A+BBecton, Dickinson and Company · 2015
- Descendant · cites it directly · 10 of its ownK152870 BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kitBecton, Dickinson and Co. · 2015
- Descendant · cites it directly · 9 of its ownK160161 BD Veritor System for Rapid Detection of Flu A + B CLIA waived kitBecton, Dickinson & CO · 2016
- Descendant · cites it directly · 5 of its ownK180438 BD Veritor System for Rapid Detection of Flu A + B CLIA waived kitBd · 2018 · Recalled
- Descendant · cites it directly · 3 of its ownK133138 BD Veritor™ System Flu A+B AssayBecton, Dickinson & CO · 2013
Showing 5 of 17 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 17 · See all- K151291BD Veritor (TM) System for the Rapid Detection of Flu A+BBecton, Dickinson and Company · 2015 · cites it directly11descendants
- K152870BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kitBecton, Dickinson and Co. · 2015 · cites it directly10descendants
- K160161BD Veritor System for Rapid Detection of Flu A + B CLIA waived kitBecton, Dickinson & CO · 2016 · cites it directly9descendants
- K180438BD Veritor System for Rapid Detection of Flu A + B CLIA waived kitBd · 2018 · cites it directly5descendants
- K133138BD Veritor™ System Flu A+B AssayBecton, Dickinson & CO · 2013 · cites it directly3descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −8 | K902609 | Directigen Flu a | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1990 | — |
| −7 | K981651 | AB Flu Oia | Biostar, Inc. | 1998 | — |
| −6 | K023556 | Flu Oia a/B Test Kit | Thermo Biostar, Inc. | 2003 | 1 |
| −5 | K031899 | Quickvue Influenza a+B Test | Quidel Corp. | 2003 | — |
| −4 | K053146 | Quickvue Influenza a + B Test | Quidel Corp. | 2005 | — |
| −3 | K092698 | Quickvue Influenza a+B Test | Quidel Corp. | 2009 | — |
| −2 | K112277 | BD Veritor (TM) System for Rapid Detection of Flu a+B | Becton, Dickinson and Company | 2011 | 1 |
| −1 | K132259 | BD Veritor System for the Rapid Detection of Flu a+B | Becton, Dickinson and Company | 2013 | — |
| 0 (this device) | K132692 | BD Veritor System for the Rapid Detection of Flu a+B | Becton, Dickinson and Company | 2013 | — |
| +1 | K151291 | BD Veritor (TM) System for the Rapid Detection of Flu A+B | Becton, Dickinson and Company | 2015 | — |
| +1 | K152870 | BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kit | Becton, Dickinson and Co. | 2015 | — |
| +1 | K160161 | BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit | Becton, Dickinson & CO | 2016 | — |
| +1 | K180438 | BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit | Bd | 2018 | 2 |
| +1 | K133138 | BD Veritor™ System Flu A+B Assay | Becton, Dickinson & CO | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1999 | 1 | 0 |
| 2000 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 2 | 0 |
| 2015 | 4 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2018 | 2 | 0 |
| 2020 | 1 | 0 |
| 2023 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 1 | 0 |
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 PSZ? 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 PSZ device
- #1 K252283 Nano-Check Influenza A+B Testscore 14.9 · 15 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K112277 | BD Veritor (TM) System for Rapid Detection of Flu a+BSummary page 1…21 CFR 866.3330 CLASSIFICATION: PREDICATE DEVICES: BD Veritor TM System for Rapid Detection of Flu A+1 POC kit (k1 12277, k132239) INTENDED USE: POC Kit The BID Veritor TM System for Rapid Detection of Flu A+B is a rapid chromatographic immunoassa… | 2011 |
| * | K132259 | BD Veritor System for the Rapid Detection of Flu a+B Our reading of the summary gave K132239, FDA’s number for Comprehensive Reverse Shoulder Screws (Biomet Manufacturing Corp). Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “BD Veritor System for Rapid Detection of Flu A+B POC kit”. | 2013 |
What descends from it? (17)
See all 177 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K151291 | BD Veritor (TM) System for the Rapid Detection of Flu A+B | 2015 | 11 |
| K152870 | BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kit | 2015 | 10 |
| K160161 | BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit | 2016 | 9 |
| K180438 | BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit | 2018 | 5 |
| K133138 | BD Veritor™ System Flu A+B Assay | 2013 | 3 |
| K223016 | BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived Kit | 2023 | 2 |
| K133140 | BD Veritor System for the Rapid Detection of RSV | 2013 | 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?
- The line of descent spans 23 years and passes through 5 companies; a new generation was cleared every 2.3 years on median.
- 2 of the 10 ancestors have a recall of any class.
- Of its descendants, K151291 (Becton, Dickinson and Company, 2015) has gone furthest, with 11 descendants of its own.
- 7 other devices also cite its predicate K112277.
How does its category compare?
All PSZ devicesPSZ Devices Detecting Influenza A, B, And C Virus Antigens: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · PSZ
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · PSZ
28in 2018
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · PSZ
1in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · PSZ
60in 2025
MAUDE reports naming product code PSZ, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 2 | — | 0 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 7 | 20 | 0 | 0 |
| 2010 | 5 | 29 | 0 | 0 |
| 2011 | 3 | 80 | 0 | 0 |
| 2012 | 2 | — | 0 | 0 |
| 2013 | 8 | 28 | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 4 | 27 | 0 | 0 |
| 2016 | 3 | 29 | 0 | 0 |
| 2017 | 3 | 200 | 0 | 0 |
| 2018 | 5 | 28 | 0 | 1 |
| 2019 | 0 | — | 0 | 1 |
| 2020 | 2 | — | 1 | 5 |
| 2021 | 0 | — | 0 | 42 |
| 2022 | 0 | — | 1 | 10 |
| 2023 | 2 | — | 0 | 12 |
| 2024 | 0 | — | 0 | 16 |
| 2025 | 2 | — | 0 | 60 |
| 2026 | 2 | — | 0 | — |
What is it indicated for?
The BD Veritor m System for Rapid Detection of Flu A+B is a rapid chromatographic immunoassay for the direct and qualitative detection of influenza A and 8 viral nucleoprotein antigens from nasal and nasopharyngeal swabs of symptomatic patients. The BID Veritor System for Rapid Detection of Flu A+B3 (also referred to as the SID Veritor System and BD Veritor System Flu A+B) is a differentiated test, such that influenza A viral antigens can be…
Read the full statement (300 words)
The BD Veritor m System for Rapid Detection of Flu A+B is a rapid chromatographic immunoassay for the direct and qualitative detection of influenza A and 8 viral nucleoprotein antigens from nasal and nasopharyngeal swabs of symptomatic patients. The BID Veritor System for Rapid Detection of Flu A+B3 (also referred to as the SID Veritor System and BD Veritor System Flu A+B) is a differentiated test, such that influenza A viral antigens can be distinguished from influenza B viral antigens from a single processed sample using a single device. The test isto be used as an aid inthe diagnosis of influenza A and B viral infections. A negative test is presumptive and it is recommended that these results be confirmed by viral culture or an FDA-cleared influenza A and B molecular assay. Negative test results do not preclude influenza viral infection and should not be used as the sole basis for treatment or other patient management decisions. The test is not intended to detect influenza C antigens.
Performance characteristics for Influenza Aand B were established during January through March of 2011 when influenza viruses A/2009 HiNi, A/H3N2, S/Victoria lineage, and 5/Yamagata lineage were the predominant influenza viruses in circulation according to the Morbidity and Modtality Weekly Report from the CDC entitled "Update: Influenza Activity-United States, 2010-2011 Season, and Composition of the 2011-2012 Influenza Vaccine." Performance characteristics may vary against other emerging influenza viruses.
If infection with a novel influenza 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 far novel virulent influenza viruses and sent to the state or local health department for testing. Virus 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.
https://510kreport.com/device/K132692 · printed Nov 6, 2026
Cite this page
510(k) Report. “K132692: BD Veritor System for the Rapid Detection of Flu a+B.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K132692
Report an extraction error
Are you the manufacturer?
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