510(k) Report

510(k) · Cleared

Cleared

VITEK 2 AST-Gram Positive Delafloxacin (<=0.015 - >=1 µg/mL)

K200590510(k) TraditionalCleared Apr 28, 202053-day reviewClass II21 CFR 866.1645

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

bioMerieux, Inc. · LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

Cleared on Apr 28, 2020 as substantially equivalent to K190616 (bioMerieux, Inc., 2019) after a 53-day review. Its family tree reaches back 4 generations to 2003.

Decided
Apr 28, 2020
Review
53 days
Class
Class II
Product code
LON
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K032766 (2003). No later device cites it as a predicate yet.

K032766 · Vitek 2 Gram Positive Linezolid · bioMerieux, Inc. · 2003K122547 · Gram Postitve Clindamycin · bioMerieux, Inc. · 2012K141149 · Vitek 2 Ast GP Ceftaroline · bioMerieux, Inc. · 2014K190616 · VITEK 2 AST-Gram Positive Dalbavancin (<= 0.015 - >= 1 µg/mL) · bioMerieux, Inc. · 201920002005201020152020
K190616 · VITEK 2 AST-Gram Positive Dalbavancin (<= 0.015 - >= 1 µg/mL) · bioMerieux, Inc. · 2019K141149 · Vitek 2 Ast GP Ceftaroline · bioMerieux, Inc. · 2014K122547 · Gram Postitve Clindamycin · bioMerieux, Inc. · 2012K032766 · Vitek 2 Gram Positive Linezolid · bioMerieux, Inc. · 20030
  1. Root · 4 generations backK032766 Vitek 2 Gram Positive LinezolidbioMerieux, Inc. · 2003
  2. 3 generations backK122547 Gram Postitve ClindamycinbioMerieux, Inc. · 2012
  3. 2 generations backK141149 Vitek 2 Ast GP CeftarolinebioMerieux, Inc. · 2014
  4. 1 generation backK190616 VITEK 2 AST-Gram Positive Dalbavancin (<= 0.015 - >= 1 µg/mL)bioMerieux, Inc. · 2019
  5. This deviceK200590 VITEK 2 AST-Gram Positive Delafloxacin (<=0.015 - >=1 µg/mL)bioMerieux, Inc. · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K032766Vitek 2 Gram Positive LinezolidbioMerieux, Inc.2003—
−3K122547Gram Postitve ClindamycinbioMerieux, Inc.2012—
−2K141149Vitek 2 Ast GP CeftarolinebioMerieux, Inc.2014—
−1K190616VITEK 2 AST-Gram Positive Dalbavancin (<= 0.015 - >= 1 µg/mL)bioMerieux, Inc.2019—
0 (this device)K200590VITEK 2 AST-Gram Positive Delafloxacin (<=0.015 - >=1 µg/mL)bioMerieux, Inc.2020—
FIG. 1 — Lineage of K200590, 2003–2020Source: 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 LON? 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 LON device

  1. #1 K260619 VITEK 2 AST-Streptococcus Cefepime (<=0.06 –…score 13.3 · 5 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
*K190616VITEK 2 AST-Gram Positive Dalbavancin (<= 0.015 - >= 1 µg/mL)
Summary page 3
…oxacin (≤0.015 - ≥1 μg/mL) C. Predicate Device: VITEK® 2 AST-Gram Positive Dalbavancin (≤0.015 - ≥1 μg/mL) (K190616) D. Device Description: The principle of the VITEK® 2 AST cards is based on the microdilution minimum inhibitory concentration (…
bioMerieux, Inc.2019—

Also cleared against K190616: 2 other devices →

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?

  • The line of descent spans 17 years and passes through 1 company; a new generation was cleared every 5.0 years on median.
  • None of the 4 ancestors has a recall.
  • 2 other devices also cite its predicate K190616.

How does its category compare?

All LON devices

LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · LON

5in 2025

2007: 192008: 72009: 82010: 12011: 82012: 102013: 72014: 42016: 32017: 102018: 42019: 82020: 52021: 52022: 82023: 112024: 22025: 52026 (partial year): 4
2007high 19 (2007) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LON

90in 2025

2007: 50 days median2008: 66 days median2009: 76 days median2011: 85 days median2012: 200 days median2013: 115 days median2014: 90 days median2016: 242 days median2017: 89 days median2018: 88 days median2019: 84 days median2020: 81 days median2021: 268 days median2022: 189 days median2023: 210 days median2025: 90 days median2026 (partial year): 146 days median
2007high 268 (2021) · low 50 (2007)2026

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

Recalls per year · LON

1in 2025

2008: 12010: 1162011: 32012: 32014: 2, 2 Class I2016: 22017: 12018: 62019: 12020: 82022: 152024: 12025: 12026 (partial year): 6
2007high 116 (2010) · low 0 (2007)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · LON

690in 2025

2007: 32008: 12010: 32011: 42012: 92013: 32014: 102015: 412016: 942017: 1972018: 5122019: 3152020: 2182021: 2322022: 1802023: 4532024: 4182025: 690
2007high 690 (2025) · low 0 (2009)2025

MAUDE reports naming product code LON, 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
2007195003
200876611
200987600
20101—1163
201188534
20121020039
2013711503
20144902 (2)10
20150—041
20163242294
201710891197
20184886512
20198841315
20205818218
202152680232
2022818915180
2023112100453
20242—1418
20255901690
202641466—

What is it indicated for?

VITEK® 2 AST-Gram Positive Delafloxacin is designed for antimicrobial susceptibility testing of Gram positive microorganisms and is intended for use with the VITEK® 2 and VITEK® 2 Compact Systems as a laboratory aid in the determination of in vitro susceptibility to antimicrobial agents. VITEK® 2 AST-Gram Positive Delafloxacin is a quantitative test. Delafloxacin has been shown to be active against most strains of the microorganisms listed below…

Read the full statement (152 words)

VITEK® 2 AST-Gram Positive Delafloxacin is designed for antimicrobial susceptibility testing of Gram positive microorganisms and is intended for use with the VITEK® 2 and VITEK® 2 Compact Systems as a laboratory aid in the determination of in vitro susceptibility to antimicrobial agents. VITEK® 2 AST-Gram Positive Delafloxacin is a quantitative test. Delafloxacin has been shown to be active against most strains of the microorganisms listed below, according to the FDA label for this antimicrobial.

Active in vitro and in clinical infections:

Acute Bacterial Skin and Skin Structure Infections (ABSSSI):

Staphylococcus aureus (including methicillin-resistant and methicillin-susceptible isolates)

Streptococcus agalactiae

Enterococcus faecalis

Community-Acquired Bacterial Pneumonia (CABP):

Staphylococcus aureus (methicillin-susceptible isolates only)

The VITEK® 2 Gram-positive Susceptibility Card is intended for use with the VITEK® 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed.

Indications for use as stated in the FDA summary.

Also cleared against K190616

2 other devices cite the same predicate.

  • K212243VITEK 2 AST- Gram Positive Telavancin (<=0.015 - >=1 µg/mL)bioMerieux, Inc. · 2022
  • K202396VITEK 2 AST-Gram Positive Fosfomycin (<=8 - >=256 ug/mL)bioMerieux, Inc. · 2021

More from bioMerieux, Inc.

281 FDA decisions under this applicant name. See the company

  • K260283VITEK 2 AST-Streptococcus Meropenem (=0.06 - =4 µg/mL)bioMerieux, Inc. · 2026
  • K260160VITEK REVEAL GN AST Assay and VITEK REVEAL AST SystembioMerieux, Inc. · 2026
  • K260282VITEK 2 AST-Streptococcus Inducible Clindamycin ResistancebioMerieux, Inc. · 2026
  • K251579VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL)bioMerieux, Inc. · 2025
  • K234012Vitek Compact ProbioMerieux, Inc. · 2025

Recent decisions in LON

The LON category page

  • K260283VITEK 2 AST-Streptococcus Meropenem (=0.06 - =4 µg/mL)bioMerieux, Inc. · 2026
  • K260619VITEK 2 AST-Streptococcus Cefepime (<=0.06 – >=4 µg/mL)Biomérieux, Inc. · 2026
  • K260282VITEK 2 AST-Streptococcus Inducible Clindamycin ResistancebioMerieux, Inc. · 2026
  • K260281VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL)Biomerieux · 2026
  • K251579VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL)bioMerieux, Inc. · 2025

https://510kreport.com/device/K200590 · printed Nov 5, 2026

Cite this page

510(k) Report. “K200590: VITEK 2 AST-Gram Positive Delafloxacin (<=0.015 - >=1 µg/mL).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K200590

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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