510(k) Report

510(k) · Cleared

Cleared

BUHLMANN fCAL turbo

K190784510(k) TraditionalCleared Jun 25, 201990-day reviewClass II21 CFR 866.5180

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

Buhlmann Laboratories AG · NXO Calprotectin, Fecal

Cleared on Jun 25, 2019 as substantially equivalent to K181012 (Buhlmann Laboratories AG, 2018) after a 90-day review. Its family tree reaches back 4 generations to 2006. 2 later devices descend from it.

Decided
Jun 25, 2019
Review
90 days
Class
Class II
Product code
NXO
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to DEN060001 (2006). 2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2019: 1 descendant cleared2024: 1 descendant clearedDEN060001 · Phical Test · Genova Diagnostics · 2006K130945 · Calprest · Eurospital S.P.A. · 2014K160447 · Calprest NG · Eurospital S.P.A. · 2016K181012 · BUHLMANN fCAL ELISA · Buhlmann Laboratories AG · 201820052010201520202025
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 1 descendant K181012 · BUHLMANN fCAL ELISA · Buhlmann Laboratories AG · 2018K160447 · Calprest NG · Eurospital S.P.A. · 2016K130945 · Calprest · Eurospital S.P.A. · 2014DEN060001 · Phical Test · Genova Diagnostics · 20060
  1. Root · 4 generations backDEN060001 Phical TestGenova Diagnostics · 2006
  2. 3 generations backK130945 CalprestEurospital S.P.A. · 2014
  3. 2 generations backK160447 Calprest NGEurospital S.P.A. · 2016
  4. 1 generation backK181012 BUHLMANN fCAL ELISABuhlmann Laboratories AG · 2018
  5. This deviceK190784 BUHLMANN fCAL turboBuhlmann Laboratories AG · 2019
  6. Descendant · cites it directly · 1 of its ownK191718 Buhlmann fCAL turbo and CALEX CapBuhlmann Laboratories AG · 2019
  7. Descendant · 2 generations on · 0 of its ownK232057 BÜHLMANN fCAL® turbo and CALEX® CapBühlmann Laboratories AG · 2024

Most influential descendants

Showing 2 of 2 · See all
  • K191718Buhlmann fCAL turbo and CALEX CapBuhlmann Laboratories AG · 2019 · cites it directly1descendant
  • K232057BÜHLMANN fCAL® turbo and CALEX® CapBühlmann Laboratories AG · 2024 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4DEN060001Phical TestGenova Diagnostics2006—
−3K130945CalprestEurospital S.P.A.2014—
−2K160447Calprest NGEurospital S.P.A.2016—
−1K181012BUHLMANN fCAL ELISABuhlmann Laboratories AG2018—
0 (this device)K190784BUHLMANN fCAL turboBuhlmann Laboratories AG2019—
+1K191718Buhlmann fCAL turbo and CALEX CapBuhlmann Laboratories AG2019—
+2K232057BÜHLMANN fCAL® turbo and CALEX® CapBühlmann Laboratories AG2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202410
FIG. 1 — Lineage of K190784, 2006–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 NXO? 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 NXO device

  1. #1 K232057 BÜHLMANN fCAL® turbo and CALEX® Capscore 8.3 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

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
*K181012BUHLMANN fCAL ELISA
Summary page 4
…NXO Device Classification II III. Predicate Device Substantial equivalence is claimed to the following device: • BÜHLMANN fCAL® ELISA, K181012, BÜHLMANN Laboratories AG IV. Device Description The BÜHLMANN fCAL® turbo, a particle-enhanced turbidimetric immunoassay…
Buhlmann Laboratories AG2018—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K191718Buhlmann fCAL turbo and CALEX CapBuhlmann Laboratories AG20191

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 13 years and passes through 3 companies; a new generation was cleared every 2.8 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K191718 (Buhlmann Laboratories AG, 2019) has gone furthest, with 1 descendant of its own.

How does its category compare?

All NXO devices

NXO Calprotectin, Fecal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · NXO

1in 2024

2014: 12016: 12017: 12018: 32019: 52022: 12023: 12024: 1
2007high 5 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NXO

90in 2019

2018: 90 days median2019: 90 days median
2007high 90 (2018)2026

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

Recalls per year · NXO

2in 2025

2024: 12025: 2
2007high 2 (2025) · low 0 (2007)2026

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

Adverse event reports per year · NXO

1in 2022

2022: 1
2007high 1 (2022) · low 0 (2007)2025

MAUDE reports naming product code NXO, 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
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20141—00
20150—00
20161—00
20171—00
201839000
201959000
20200—00
20210—00
20221—01
20231—00
20241—10
20250—20
20260—0—

What is it indicated for?

The BÜHLMANN fCAL® turbo is an in vitro diagnostic assay intended for the quantitative measurement of fecal calprotectin, a neutrophilic protein that is a marker of intestinal mucosal inflammation, in human stool. The BÜHLMANN fCAL® turbo aids in the diagnosis of inflammatory bowel disease (IBD), specifically Crohn’s disease (CD) and ulcerative colitis (UC) and aids in the differentiation of IBD from irritable bowel syndrome (IBS) in conjunction with other laboratory and clinical findings.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K190784: BUHLMANN fCAL turbo.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K190784

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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