510(k) Report

510(k) · Cleared

Cleared

Roche Diagnostics, Boehringer Mannheim Corporation Inorganic Phosphorus Reagent Catalog Number 1730347

K983503510(k) TraditionalCleared Dec 1, 199856-day reviewClass I21 CFR 862.1580

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

Boehringer Mannheim Corp. · CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

Cleared on Dec 1, 1998 after a 56-day review. The FDA summary names its predicate without a number.

Decided
Dec 1, 1998
Review
56 days
Class
Class I
Product code
CEO
Recalls
None
Predicates
0

The FDA summary names its predicate without a number.

FIG. 1 — Lineage of K983503Source: FDA 510(k) database · 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.

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  • 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
*—Roche Diagnostics, Boehringer Mannheim Phosphorus (inorganic) test system
Named without a submission number
—

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.

How does its category compare?

All CEO devices

CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CEO

1in 2011

2008: 12011: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CEO

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

Recalls per year · CEO

1in 2025

2007: 12010: 12012: 12013: 32025: 1
2007high 3 (2013) · low 0 (2008)2026

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

Adverse event reports per year · CEO

8in 2025

2007: 132008: 12010: 412011: 192013: 12014: 12015: 32017: 42018: 22019: 22020: 22021: 32022: 22023: 52024: 52025: 8
2007high 41 (2010) · low 0 (2009)2025

MAUDE reports naming product code CEO, 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—113
20081—01
20090—00
20100—141
20111—019
20120—10
20130—31
20140—01
20150—03
20160—00
20170—04
20180—02
20190—02
20200—02
20210—03
20220—02
20230—05
20240—05
20250—18
20260—0—

What is it indicated for?

The Roche Diagnostics, Boehringer Mannheim Inorganic Phosphorus reagent is intended for use for the quantitative in vitro determination of phosphorus in human serum, plasma and urine with automated clinical chemistry analyzers.

According to the Code of Federal Regulations, Title 21 (Food and Drugs), Part 862.1580, a Phosphorus (inorganic) test system is a device intended to measure inorganic phosphorus in serum, plasma, and urine. Measurements of phosphorus (inorganic) are used in the diagnosis and treatment of various disorders, including parathyroid gland and kidney diseases, and vitamin D imbalance.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K983503: Roche Diagnostics, Boehringer Mannheim Corporation Inorganic Phosphorus Reagent Catalog Number 1730347.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K983503

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026