510(k) Report

510(k) · Cleared

Cleared

ACL TOP Family 50 Series (ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS; ACL TOP 550 CTS; ACL TOP 350 CTS)

K242127510(k) SpecialCleared Aug 16, 202428-day reviewClass II21 CFR 864.5400

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

Instrumentation Laboratory (IL) Co. · GKP Instrument, Coagulation, Automated

Cleared on Aug 16, 2024 as substantially equivalent to K150877 (Instrumentation Laboratory CO, 2015) after a 28-day review. Its family tree reaches back 6 generations to 2000.

Decided
Aug 16, 2024
Review
28 days
Class
Class II
Product code
GKP
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K002400 (2000). No later device cites it as a predicate yet.

  1. Root · 6 generations backK002400 Modification of Acl AdvanceInstrumentation Laboratory CO · 2000 · Recalled
  2. 5 generations backK033414 Acl Top Model, TopInstrumentation Laboratory CO · 2004 · Recalled
  3. 4 generations backK063679 Acl TopInstrumentation Laboratory CO · 2007 · Recalled
  4. 3 generations backK073377 Acl Top (with System Software V3.0.0)Instrumentation Laboratory CO · 2008
  5. 2 generations backK091980 Acl Top 700 LasInstrumentation Laboratory CO · 2009 · Recalled
  6. 1 generation backK150877 Acl Top Family 50 Series: Acl Top 350 CTS; Acl Top 550 CTS; Acl Top…Instrumentation Laboratory CO · 2015 · Recalled
  7. This deviceK242127 ACL TOP Family 50 Series (ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750…Instrumentation Laboratory (IL) Co. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K002400Modification of Acl AdvanceInstrumentation Laboratory CO20002
−5K033414Acl Top Model, TopInstrumentation Laboratory CO20041
−4K063679Acl TopInstrumentation Laboratory CO20071
−3K073377Acl Top (with System Software V3.0.0)Instrumentation Laboratory CO2008—
−2K091980Acl Top 700 LasInstrumentation Laboratory CO200924
−1K150877Acl Top Family 50 Series: Acl Top 350 CTS; Acl Top 550 CTS; Acl Top 750; Acl…Instrumentation Laboratory CO20151
0 (this device)K242127ACL TOP Family 50 Series (ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS; ACL…Instrumentation Laboratory (IL) Co.2024—
FIG. 1 — Lineage of K242127, 2000–2024Source: 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 GKP? 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 GKP device

  1. #1 K231031 ACL TOP Family 70 Seriesscore 7.0 · 6 generations · no Class I recall
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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
*K150877Acl Top Family 50 Series: Acl Top 350 CTS; Acl Top 550 CTS; Acl Top 750; Acl Top 750…
Summary page 4
…0 • ACL TOP 750 CTS • ACL TOP 750 LAS Predicate Device ACL TOP Family 50 Series K150877 Regulation Section No. 21 CFR 864.5400 Regulation Descriptio…
Instrumentation Laboratory CO20151
†K231031ACL TOP Family 70 SeriesInstrumentation Laboratory Company2023—

Also cleared against K150877: 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 24 years and passes through 2 companies; a new generation was cleared every 3.4 years on median.
  • 5 of the 6 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K150877.

How does its category compare?

All GKP devices

GKP Instrument, Coagulation, Automated: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · GKP

1in 2024

2007: 12008: 12009: 12015: 12016: 12023: 12024: 1
2007high 1 (2007) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GKP

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

Recalls per year · GKP

1in 2022

2007: 32010: 42022: 1
2007high 4 (2010) · low 0 (2008)2026

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

Adverse event reports per year · GKP

5in 2024

2007: 32008: 52009: 1902010: 742011: 452012: 352013: 422014: 262015: 242016: 132017: 182018: 192019: 382020: 142021: 172022: 42023: 42024: 5
2007high 190 (2009) · low 0 (2025)2025

MAUDE reports naming product code GKP, 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
20071—33
20081—05
20091—0190
20100—474
20110—045
20120—035
20130—042
20140—026
20151—024
20161—013
20170—018
20180—019
20190—038
20200—014
20210—017
20220—14
20231—04
20241—05
20250—00
20260—0—

What is it indicated for?

The ACL TOP Family 50 Series (ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS; ACL TOP 550 CTS; ACL TOP 350 CTS) are bench top, fully automated, random access analyzers designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K242127: ACL TOP Family 50 Series (ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS; ACL TOP 550 CTS; ACL TOP 350 CTS).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K242127

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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