510(k) Report

510(k) · Cleared

Cleared

Roche Reagent for Calcium

K883453510(k) TraditionalCleared Oct 25, 198874-day reviewClass II21 CFR 862.1145

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

Roche Diagnostic Systems, Inc. · CJY Azo Dye, Calcium

Cleared on Oct 25, 1988 after a 74-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Oct 25, 1988
Review
74 days
Class
Class II
Product code
CJY
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2006: 1 descendant cleared2011: 1 descendant cleared1990200020102020
  1. This deviceK883453 Roche Reagent for CalciumRoche Diagnostic Systems, Inc. · 1988
  2. Descendant · cites it directly · 1 of its ownK060205 General Chemistries on Abx Pentra 400 Clinical Chemistry AnalyzerHoriba Abx · 2006 · Recalled
  3. Descendant · 2 generations on · 0 of its ownK100263 Elitech Clinical Systems Phosphorus, Uric Acid Mono SL and Urea UV…Seppim S.A.S. · 2011

Most influential descendants

Showing 2 of 2 · See all
  • K060205General Chemistries on Abx Pentra 400 Clinical Chemistry AnalyzerHoriba Abx · 2006 · cites it directly1descendant
  • K100263Elitech Clinical Systems Phosphorus, Uric Acid Mono SL and Urea UV SL ReagentsSeppim S.A.S. · 2011 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K883453Roche Reagent for CalciumRoche Diagnostic Systems, Inc.1988—
+1K060205General Chemistries on Abx Pentra 400 Clinical Chemistry AnalyzerHoriba Abx20062
+2K100263Elitech Clinical Systems Phosphorus, Uric Acid Mono SL and Urea UV SL ReagentsSeppim S.A.S.2011—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
201110
FIG. 1 — Lineage of K883453, 1988–2011Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in CJY? 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 CJY device

  1. #1 K244042 Calcium2score 9.4 · 3 generations · no Class I recall
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K060205General Chemistries on Abx Pentra 400 Clinical Chemistry AnalyzerHoriba Abx20061

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?

  • Of its descendants, K060205 (Horiba Abx, 2006) has gone furthest, with 1 descendant of its own.

How does its category compare?

All CJY devices

CJY Azo Dye, Calcium: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CJY

1in 2025

2007: 22008: 22009: 12012: 12013: 12015: 12018: 12019: 12025: 1
2007high 2 (2007) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CJY

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

Recalls per year · CJY

1in 2022

2013: 42018: 22022: 1
2007high 4 (2013) · low 0 (2007)2026

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

Adverse event reports per year · CJY

59in 2025

2007: 32008: 42009: 82010: 102011: 92012: 52013: 82014: 52015: 42016: 32017: 262018: 212019: 292020: 332021: 242022: 172023: 292024: 342025: 59
2007high 59 (2025) · low 3 (2007)2025

MAUDE reports naming product code CJY, 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
20072—03
20082—04
20091—08
20100—010
20110—09
20121—05
20131—48
20140—05
20151—04
20160—03
20170—026
20181—221
20191—029
20200—033
20210—024
20220—117
20230—029
20240—034
20251—059
20260—0—
Cite this page

510(k) Report. “K883453: Roche Reagent for Calcium.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K883453

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026