510(k) Report

510(k) · Cleared

Cleared

Immulite 2000; Cortisol Calibration Verification Material, Folic Acid Calibration Verification Material, Vitamin B12 Cal

K141444510(k) AbbreviatedCleared Jul 9, 201437-day reviewClass I21 CFR 862.1660

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

Siemens Healthcare Diagnostics, Inc. · JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Cleared on Jul 9, 2014 as substantially equivalent to K133124 (Siemens Healthcare Diagnostics, Inc., 2013) and 1 other predicate after a 37-day review. Its family tree reaches back 7 generations to 1995. 1 later device descends from it.

Decided
Jul 9, 2014
Review
37 days
Class
Class I
Product code
JJX
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K950469 (1995). 24 ancestors in all, the oldest K910440 (1991). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2013: 1 other ancestor2011: 2 other ancestors2002: 1 other ancestor2010: 2 other ancestors2009: 1 other ancestor1996: 1 other ancestor1995: 1 other ancestor2004: 1 other ancestor2001: 1 other ancestor1998: 3 other ancestors1992: 1 other ancestor2003: 1 other ancestor1991: 1 other ancestor2015: 1 descendant clearedK950469 · Document Serum Multianalyte Calibration Verification Test Set · Casco Standards · 1995K992034 · Document Thyroid Cal*Ver · Casco-Nerl Diagnostics Corporation (Maine) · 1999K062501 · Validate Thyroid Calibration Verification / Linearity Test Set, Model 901 · Maine Standards Co. · 2006K102904 · Enhanced Estradiol (EE2) Master Curve Material · Siemens Healthcare Diagnostics · 2010K110061 · CVM, Unconjugated Estriol (UE3) Calibration Verification Material · Siemens Healthcare Diagnostics · 2011×2: 2 generations cleared close together, K133128 (2013), K140258 (2014) 1990200020102020
  1. Root · 7 generations backK950469 Document Serum Multianalyte Calibration Verification Test SetCasco Standards · 1995
  2. 6 generations backK992034 Document Thyroid Cal*VerCasco-Nerl Diagnostics Corporation (Maine) · 1999
  3. 5 generations backK062501 Validate Thyroid Calibration Verification / Linearity Test Set…Maine Standards Co. · 2006
  4. 4 generations backK102904 Enhanced Estradiol (EE2) Master Curve MaterialSiemens Healthcare Diagnostics · 2010
  5. 3 generations backK110061 CVM, Unconjugated Estriol (UE3) Calibration Verification MaterialSiemens Healthcare Diagnostics · 2011
  6. 2 generations backK133128 Immulite 2000; HCG Calibration Verification Material, Insulin…Siemens Healthcare Diagnostics, Inc. · 2013
  7. 1 generation backK140258 Immulite 2000 Dhea-SO4; Third Generation TSH and Intact PTH…Siemens Healthcare Diagnostics, Inc. · 2014
  8. This deviceK141444 Immulite 2000; Cortisol Calibration Verification Material, Folic…Siemens Healthcare Diagnostics, Inc. · 2014
  9. Descendant · cites it directly · 0 of its ownK143636 IMMULITE 2000 Androstenedione Calibration Verification Material…Siemens Healthcare Diagnostics, Inc. · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K143636IMMULITE 2000 Androstenedione Calibration Verification Material, IMMULITE 2000 Troponin…Siemens Healthcare Diagnostics, Inc. · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K950469Document Serum Multianalyte Calibration Verification Test SetCasco Standards1995—
−6K992034Document Thyroid Cal*VerCasco-Nerl Diagnostics Corporation (Maine)1999—
−5K062501Validate Thyroid Calibration Verification / Linearity Test Set, Model 901Maine Standards Co.2006—
−4K102904Enhanced Estradiol (EE2) Master Curve MaterialSiemens Healthcare Diagnostics2010—
−3K110061CVM, Unconjugated Estriol (UE3) Calibration Verification MaterialSiemens Healthcare Diagnostics2011—
−2K133128Immulite 2000; HCG Calibration Verification Material, Insulin Calibration…Siemens Healthcare Diagnostics, Inc.2013—
−1K140258Immulite 2000 Dhea-SO4; Third Generation TSH and Intact PTH Calibration…Siemens Healthcare Diagnostics, Inc.2014—
0 (this device)K141444Immulite 2000; Cortisol Calibration Verification Material, Folic Acid…Siemens Healthcare Diagnostics, Inc.2014—
+1K143636IMMULITE 2000 Androstenedione Calibration Verification Material, IMMULITE 2000…Siemens Healthcare Diagnostics, Inc.2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199210
199510
199610
199830
200110
200210
200310
200410
200910
201020
201120
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
FIG. 1 — Lineage of K141444, 1995–2015Source: 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 JJX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K133124Immulite 2000; Total T3 Calibration Verification Material, Total T4 Calibration…
Summary page 1
…te Device Name IMMULITE®R 2000 Total T3 Calibration Verification Material (CVM) Predicate 510(k) No: K133 124 4. Device Description: The IMMULITE® 2000 Cortisol Calibration Verification Material…
Siemens Healthcare Diagnostics, Inc.2013—
*K140258Immulite 2000 Dhea-SO4; Third Generation TSH and Intact PTH Calibration Verification…
Summary page 5
…e Device Name IMMULITE 2000 DHEA-S04 Calibration Verification Material (CVM) Predicate 510(k) No: K140258 4. Device Description: The IMMULITEO 2000 Folic Acid Calibration Verification…
Siemens Healthcare Diagnostics, Inc.2014—

Also cleared against K133124: 2 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K143636IMMULITE 2000 Androstenedione Calibration Verification Material, IMMULITE 2000 Troponin…Siemens Healthcare Diagnostics, Inc.20150

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 19 years and passes through 5 companies; a new generation was cleared every 2.1 years on median.
  • 1 of the 24 ancestors has a recall of any class.
  • Of its descendants, K143636 (Siemens Healthcare Diagnostics, Inc., 2015) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K133124.

How does its category compare?

All JJX devices

JJX Single (Specified) Analyte Controls (Assayed And Unassayed): FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · JJX

2in 2017

2007: 62008: 82009: 172010: 242011: 192012: 152013: 192014: 222015: 112016: 62017: 2
2007high 24 (2010) · low 0 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JJX

31in 2016

2007: 53 days median2008: 52 days median2009: 80 days median2010: 80 days median2011: 62 days median2012: 40 days median2013: 37 days median2014: 30 days median2015: 65 days median2016: 31 days median
2007high 80 (2009) · low 30 (2014)2026

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

Recalls per year · JJX

1in 2021

2007: 32008: 32010: 32011: 22014: 12015: 12016: 22018: 22021: 1
2007high 3 (2007) · low 0 (2009)2026

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

Adverse event reports per year · JJX

22in 2025

2007: 22009: 12010: 62011: 622012: 322013: 512014: 482015: 672016: 372017: 192018: 352019: 822020: 772021: 432022: 242023: 222024: 302025: 22
2007high 82 (2019) · low 0 (2008)2025

MAUDE reports naming product code JJX, 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
200765332
200885230
2009178001
2010248036
20111962262
20121540032
20131937051
20142230148
20151165167
2016631237
20172—019
20180—235
20190—082
20200—077
20210—143
20220—024
20230—022
20240—030
20250—022
20260—0—

What is it indicated for?

The IMMULITE® Cortisol Calibration Verification Material is for in vitro diagnostic use in the verification of calibration of the IMMULITE Cortisol assay on the IMMULITE 2000 systems.

The IMMULITE® Folic Acid Calibration Verification Material is for in vitro diagnostic use in the verification of calibration of the IMMULITE Folic Acid assay on the IMMULITE 2000 systems.

The IMMULITE® Vitamin B12 Calibration Verification Material is for in vitro diagnostic use in the verification of calibration of the IMMULITE Vitamin B12 assay on the IMMULITE 2000 systems.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K141444: Immulite 2000; Cortisol Calibration Verification Material, Folic Acid Calibration Verification Material, Vitamin B12 Cal.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141444

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