510(k) Report

510(k) · Cleared

Cleared

nextaro® v, 20/20

K240748510(k) SpecialCleared Apr 16, 202428-day reviewClass II21 CFR 880.5440

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

Sfm Medical Devices GmbH · LHI Set, I.V. Fluid Transfer

Cleared on Apr 16, 2024 as substantially equivalent to K183187 (Sfm Medical Devices GmbH, 2019) after a 28-day review. Its family tree reaches back 2 generations to 2003.

Decided
Apr 16, 2024
Review
28 days
Class
Class II
Product code
LHI
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K031861 (2003). No later device cites it as a predicate yet.

  1. Root · 2 generations backK031861 MIX2VIAL Transfer DeviceMedimop Medical Projects, Ltd. · 2003
  2. 1 generation backK183187 nextaro Transfer System, nextaro vaSfm Medical Devices GmbH · 2019
  3. This deviceK240748 nextaro® v, 20/20Sfm Medical Devices GmbH · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K031861MIX2VIAL Transfer DeviceMedimop Medical Projects, Ltd.2003—
−1K183187nextaro Transfer System, nextaro vaSfm Medical Devices GmbH2019—
0 (this device)K240748nextaro® v, 20/20Sfm Medical Devices GmbH2024—
FIG. 1 — Lineage of K240748, 2003–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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 LHI? 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 LHI device

  1. #1 K252987 ADRx™ Admixture Devicescore 12.4 · 4 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
*K183187nextaro Transfer System, nextaro va
Summary page 5
…Intravascular Administration Set Regulation Number: 21 CFR 880.5440 Legally Marketed Predicate: nextaro® Transfer System (K183187), sfm medical devices GmbH Indications for The nextaro® v, 20/20 is indicated for t…
Sfm Medical Devices GmbH2019—

Also cleared against K183187: 1 other device →

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 21 years and passes through 2 companies; a new generation was cleared every 15.6 years on median.
  • None of the 2 ancestors has a recall.
  • 1 other device also cites its predicate K183187.

How does its category compare?

All LHI devices

LHI Set, I.V. Fluid Transfer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · LHI

6in 2025

2007: 32008: 42009: 82010: 52011: 32012: 52013: 42014: 62015: 32016: 32017: 52018: 12019: 42020: 32021: 32022: 62023: 52024: 92025: 62026 (partial year): 2
2007high 9 (2024) · low 1 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LHI

196in 2025

2007: 89 days median2008: 154 days median2009: 95 days median2010: 139 days median2011: 99 days median2012: 127 days median2013: 102 days median2014: 63 days median2015: 99 days median2016: 159 days median2017: 56 days median2019: 247 days median2020: 189 days median2021: 396 days median2022: 278 days median2023: 90 days median2024: 166 days median2025: 196 days median
2007high 396 (2021) · low 56 (2017)2026

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

Recalls per year · LHI

1in 2024

2007: 12008: 32009: 12010: 32011: 122013: 32016: 1, 1 Class I2017: 12018: 3, 3 Class I2019: 12022: 22023: 2, 2 Class I2024: 12026 (partial year): 1
2007high 12 (2011) · low 0 (2012)2026

Class I (6 since 2007) Class II/III not classified

Adverse event reports per year · LHI

1,334in 2025

2007: 182008: 272009: 372010: 492011: 1552012: 5292013: 1542014: 1552015: 1282016: 2192017: 5362018: 1,4992019: 1,6342020: 1,1712021: 9332022: 1,8342023: 1,0472024: 1,2702025: 1,334
2007high 1,834 (2022) · low 18 (2007)2025

MAUDE reports naming product code LHI, 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
2007389118
20084154327
2009895137
20105139349
201139912155
201251270529
201341023154
20146630155
20153990128
201631591 (1)219
20175561536
20181—3 (3)1,499
2019424711,634
2020318901,171
202133960933
2022627821,834
20235902 (2)1,047
2024916611,270
2025619601,334
20262—1—

What is it indicated for?

The nextaro® v, 20/20 is indicated for the transfer and mixing of drugs contained in vials.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K240748: nextaro® v, 20/20.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K240748

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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