510(k) Report

510(k) · Cleared

Cleared

Dimension Alkaline Phosphatase Flex Reagent Cartridge, Dimension Alkaline Phosphatase Calibrator

K121907510(k) TraditionalCleared Jul 23, 201224-day reviewClass II21 CFR 862.1050

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

Siemens Healthcare Diagnostics · CJO Alpha-Naphthyl Phosphate, Alkaline Phosphatase Or Isoenzymes

Cleared on Jul 23, 2012 as substantially equivalent to K991576 (Bayer Corp., 1999) and 1 other predicate after a 24-day review. Its family tree reaches back 2 generations to 1986.

Decided
Jul 23, 2012
Review
24 days
Class
Class II
Product code
CJO
Recalls
None
Predicates
2

Its longest line of descent runs back 2 generations to K860021 (1986). 3 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 2 generations backK860021 Dimension (TM) Clinical Chemistry SystemE.I. Dupont DE Nemours & Co., Inc. · 1986 · Recalled
  2. 1 generation backK061818 Dimension Vista System Alkaline Phosphatase Calibrator (Alp Cal -…Dade Behring, Inc. · 2006 · Recalled
  3. This deviceK121907 Dimension Alkaline Phosphatase Flex Reagent Cartridge, Dimension…Siemens Healthcare Diagnostics · 2012
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K860021Dimension (TM) Clinical Chemistry SystemE.I. Dupont DE Nemours & Co., Inc.19861
−1K061818Dimension Vista System Alkaline Phosphatase Calibrator (Alp Cal - KC330)Dade Behring, Inc.20061
0 (this device)K121907Dimension Alkaline Phosphatase Flex Reagent Cartridge, Dimension Alkaline…Siemens Healthcare Diagnostics2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199910
FIG. 1 — Lineage of K121907, 1986–2012Source: 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 CJO? 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? (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
*K991576Additional Assays for the Bayer Advia 1650 Chemistry System
Summary page 1
…antial equivalence to the Dimension® Alkaline Phosphatase (ALPI) Flex® reagent cartridge is the ADVIA® Chemistry Alkaline Phosphatase AMP Method previously cleared under k991576. The predicate device used to demonstrate substantial equivalence to the Dimension®D Alkaline Phosphatase Calibrator (ALPI CAL)…
Bayer Corp.19993
*K061818Dimension Vista System Alkaline Phosphatase Calibrator (Alp Cal - KC330)
Summary page 1
…te substantial equivalence to the Dimension®D Alkaline Phosphatase Calibrator (ALPI CAL) is the Dimension Vista® Alkaline Phosphatase Calibrator previously cleared under k061818. G. Device Description: The ALPI method employs alkaline phosphatase that catalyzes the transphosphorylation of…
Dade Behring, Inc.20061

Also cleared against K991576: 11 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 26 years and passes through 3 companies; a new generation was cleared every 20.4 years on median.
  • 3 of the 3 ancestors have a recall of any class.
  • 11 other devices also cite its predicate K991576.

How does its category compare?

All CJO devices

CJO Alpha-Naphthyl Phosphate, Alkaline Phosphatase Or Isoenzymes: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · CJO

2in 2012

2012: 2
2007high 2 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CJO

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

Recalls per year · CJO

1in 2020

2020: 1
2007high 1 (2020) · low 0 (2007)2026

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

Adverse event reports per year · CJO

1in 2010

2010: 1
2007high 1 (2010) · low 0 (2007)2025

MAUDE reports naming product code CJO, 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—01
20110—00
20122—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—10
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

The ALPI method is an in vitro diagnostic test for the quantitative measurement of alkaline phosphatase in human serum and plasma on the Dimension® clinical chemistry system. Measurements of alkaline phosphatase or its isoenzymes are used in the diagnosis and treatment of liver, bone, parathyroid, and intestinal diseases.

ALP! CAL is an in vitro diagnostic product for the calibration of alkaline phosphatase (ALPI) method on the Dimension® clinical chemistry system.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K121907: Dimension Alkaline Phosphatase Flex Reagent Cartridge, Dimension Alkaline Phosphatase Calibrator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K121907

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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