510(k) Report

510(k) · Cleared

Cleared

Calcium, Scal, Nortrol, Abtrol

K073355510(k) TraditionalCleared Feb 28, 200891-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

Thermofisher Scientific OY · CJY Azo Dye, Calcium

Cleared on Feb 28, 2008 as substantially equivalent to K991576 (Bayer Corp., 1999) after a 91-day review. Its family tree reaches back 1 generation to 1999.

Decided
Feb 28, 2008
Review
91 days
Class
Class II
Product code
CJY
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K991576 (1999). No later device cites it as a predicate yet.

  1. Root · 1 generation backK991576 Additional Assays for the Bayer Advia 1650 Chemistry SystemBayer Corp. · 1999 · Recalled
  2. This deviceK073355 Calcium, Scal, Nortrol, AbtrolThermofisher Scientific OY · 2008
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K991576Additional Assays for the Bayer Advia 1650 Chemistry SystemBayer Corp.19993
0 (this device)K073355Calcium, Scal, Nortrol, AbtrolThermofisher Scientific OY2008—
FIG. 1 — Lineage of K073355, 1999–2008Source: 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 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
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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
*K991576Additional Assays for the Bayer Advia 1650 Chemistry System
Summary page 2
…to other devices legally marketed in United States. We claim equivalence to the Bayer ADVIA Calcium assay (K991576). Therm, Fisher Scientific Oy Ratastic 2 +358 (9) 329 100 tel Y-tunnus 0921547-0 wwwlhcrmocor…
Bayer Corp.19993

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?

  • Its one ancestor has a recall.
  • 11 other devices also cite its predicate K991576.

How does its category compare?

All CJY devices

CJY Azo Dye, Calcium: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

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—

What is it indicated for?

The Calcium test system is intended for quantitative in vitro diagnostic measurement of calcium concentration in human serum or plasma. Calcium measurements are used in the diagnosis and treatment of parathyroid disease, a variety of bone diseases, chronic renal disease and tetany For in vitro diagnostic use on T60 instrument. sCal is used as a multicalibrator for quantitative measurements using methods defined by Thermo Fisher Scientific Oy For in vitro…

Read the full statement (165 words)

The Calcium test system is intended for quantitative in vitro diagnostic measurement of calcium concentration in human serum or plasma. Calcium measurements are used in the diagnosis and treatment of parathyroid disease, a variety of bone diseases, chronic renal disease and tetany

For in vitro diagnostic use on T60 instrument. sCal is used as a multicalibrator for quantitative measurements using methods defined by Thermo Fisher Scientific Oy

For in vitro diagnostic use for quantitative testing on T60 instrument. Nortrol is a control serum to monitor trueness and precision of the analytes listed in the separate Nortrol value sheet. The given values are valid for T60 Clinical Chemistry Instruments using methods defined by Thermo Fisher Scientific Oy.

For in vitro diagnostic use for quantitative testing on T60 instrument. Abtrol is a control serum to monitor trueness and precision of the analytes listed in the separate Abtrol value sheet. The given values are valid for T60 Clinical Chemistry Instruments using methods defined by Thermo Fisher Scientific Oy.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K073355: Calcium, Scal, Nortrol, Abtrol.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K073355

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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