510(k) Report

510(k) · Cleared

Cleared

Immulite 2000 Dhea-SO4; Third Generation TSH and Intact PTH Calibration Verification Material

K140258510(k) AbbreviatedCleared Mar 5, 201430-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 Mar 5, 2014 as substantially equivalent to K133128 (Siemens Healthcare Diagnostics, Inc., 2013) after a 30-day review. Its family tree reaches back 6 generations to 1995. 7 later devices descend from it.

Decided
Mar 5, 2014
Review
30 days
Class
Class I
Product code
JJX
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K950469 (1995). 16 ancestors in all, the oldest K910440 (1991). 7 later devices descend from it, 6 citing it directly.

  1. Root · 6 generations backK950469 Document Serum Multianalyte Calibration Verification Test SetCasco Standards · 1995
  2. 5 generations backK992034 Document Thyroid Cal*VerCasco-Nerl Diagnostics Corporation (Maine) · 1999
  3. 4 generations backK062501 Validate Thyroid Calibration Verification / Linearity Test Set…Maine Standards Co. · 2006
  4. 3 generations backK102904 Enhanced Estradiol (EE2) Master Curve MaterialSiemens Healthcare Diagnostics · 2010
  5. 2 generations backK110061 CVM, Unconjugated Estriol (UE3) Calibration Verification MaterialSiemens Healthcare Diagnostics · 2011
  6. 1 generation backK133128 Immulite 2000; HCG Calibration Verification Material, Insulin…Siemens Healthcare Diagnostics, Inc. · 2013
  7. This deviceK140258 Immulite 2000 Dhea-SO4; Third Generation TSH and Intact PTH…Siemens Healthcare Diagnostics, Inc. · 2014
  8. Descendant · cites it directly · 1 of its ownK141444 Immulite 2000; Cortisol Calibration Verification Material, Folic…Siemens Healthcare Diagnostics, Inc. · 2014
  9. Descendant · cites it directly · 0 of its ownK143373 IMMULITE® 2000 Calcitonin Calibration Verification Material…Siemens Healthcare Diagnostics, Inc. · 2015
  10. Descendant · 2 generations on · 0 of its ownK143636 IMMULITE 2000 Androstenedione Calibration Verification Material…Siemens Healthcare Diagnostics, Inc. · 2015
  11. Descendant · cites it directly · 0 of its ownK143639 IMMULITE 2000 CEA Calibration Verification MaterialSiemens Healthcare Diagnostics · 2015
  12. Descendant · cites it directly · 0 of its ownK143504 IMMULITE 2000 Albumin Calibration Verification Material, IMMULITE…Siemens Healthcare Diagnostics, Inc. · 2015

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2014: 32015: 4
2014high 4 (2015) · low 0 (2016)2026

Most influential descendants

Showing 5 of 7 · See all
  • K141444Immulite 2000; Cortisol Calibration Verification Material, Folic Acid Calibration…Siemens Healthcare Diagnostics, Inc. · 2014 · cites it directly1descendant
  • K143373IMMULITE® 2000 Calcitonin Calibration Verification Material , IMMULITE® 2000 Prostatic…Siemens Healthcare Diagnostics, Inc. · 2015 · cites it directly0descendants
  • K143636IMMULITE 2000 Androstenedione Calibration Verification Material, IMMULITE 2000 Troponin…Siemens Healthcare Diagnostics, Inc. · 2015 · 2 generations on0descendants
  • K143639IMMULITE 2000 CEA Calibration Verification MaterialSiemens Healthcare Diagnostics · 2015 · cites it directly0descendants
  • K143504IMMULITE 2000 Albumin Calibration Verification Material, IMMULITE 2000 Myoglobin…Siemens Healthcare Diagnostics, Inc. · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K950469Document Serum Multianalyte Calibration Verification Test SetCasco Standards1995—
−5K992034Document Thyroid Cal*VerCasco-Nerl Diagnostics Corporation (Maine)1999—
−4K062501Validate Thyroid Calibration Verification / Linearity Test Set, Model 901Maine Standards Co.2006—
−3K102904Enhanced Estradiol (EE2) Master Curve MaterialSiemens Healthcare Diagnostics2010—
−2K110061CVM, Unconjugated Estriol (UE3) Calibration Verification MaterialSiemens Healthcare Diagnostics2011—
−1K133128Immulite 2000; HCG Calibration Verification Material, Insulin Calibration…Siemens Healthcare Diagnostics, Inc.2013—
0 (this device)K140258Immulite 2000 Dhea-SO4; Third Generation TSH and Intact PTH Calibration…Siemens Healthcare Diagnostics, Inc.2014—
+1K141444Immulite 2000; Cortisol Calibration Verification Material, Folic Acid…Siemens Healthcare Diagnostics, Inc.2014—
+1K143373IMMULITE® 2000 Calcitonin Calibration Verification Material , IMMULITE® 2000…Siemens Healthcare Diagnostics, Inc.2015—
+2K143636IMMULITE 2000 Androstenedione Calibration Verification Material, IMMULITE 2000…Siemens Healthcare Diagnostics, Inc.2015—
+1K143639IMMULITE 2000 CEA Calibration Verification MaterialSiemens Healthcare Diagnostics2015—
+1K143504IMMULITE 2000 Albumin Calibration Verification Material, IMMULITE 2000…Siemens Healthcare Diagnostics, Inc.2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199830
200110
200310
200410
200910
201020

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201430
201540
FIG. 1 — Lineage of K140258, 1995–2015Source: 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 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
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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
*K133128Immulite 2000; HCG Calibration Verification Material, Insulin Calibration Verification…
Summary page 1
…Clinical Chemistry (75) 3. Predicate Device Name IMMULITE"' 2000 Insulin Calibration Verification Material (CVM) Predicate 510(k) No: K133 128 The Calibration Verification Material (CVM) contains one set of four 4. Device Description…
Siemens Healthcare Diagnostics, Inc.2013—

Also cleared against K133128: 6 other devices →

What descends from it? (7)

6 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K141444Immulite 2000; Cortisol Calibration Verification Material, Folic Acid Calibration…Siemens Healthcare Diagnostics, Inc.20141
K143373IMMULITE® 2000 Calcitonin Calibration Verification Material , IMMULITE® 2000 Prostatic…Siemens Healthcare Diagnostics, Inc.20150
K143639IMMULITE 2000 CEA Calibration Verification MaterialSiemens Healthcare Diagnostics20150
K143504IMMULITE 2000 Albumin Calibration Verification Material, IMMULITE 2000 Myoglobin…Siemens Healthcare Diagnostics, Inc.20150
K142878IMMULITE 2000 Beta-2 Microglobulin Calibration Verification Material, IMMULITE 2000 High…Siemens Healthcare Diagnostics, Inc.20140
K142811IMMULITE 2000 LH Calibration Verification Material (CVM), IMMULITE 2000 Free T3…Siemens Healthcare Diagnostics, Inc.20140

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 4.2 years on median.
  • None of the 16 ancestors has a recall.
  • Of its descendants, K141444 (Siemens Healthcare Diagnostics, Inc., 2014) has gone furthest, with 1 descendant of its own.
  • 6 other devices also cite its predicate K133128.

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 2000 DHEA-S04 Calibration Verification Material (CVM) is intended for in vitro diagnostic use in the verification of calibration of the IMMULITE DHEA-S04 assay on the IMMULITE 2000 systems.

The IMMULITE 2000 Third Generation TSH Calibration Verification Material (CVM) is intended for in vitro diagnostic use in the verification of calibration of the IMMULITE Third Generation TSH assay on the IMMULITE 2000 systems.

The IMMULITE 2000 Intact PTH Calibration Verification Material (CVM) is intended for in vitro diagnostic use in the verification of calibration of the IMMULITE Intact PTH assay on the IMMULITE 2000 systems.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K140258: Immulite 2000 Dhea-SO4; Third Generation TSH and Intact PTH Calibration Verification Material.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140258

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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