510(k) Report

510(k) · Cleared

Cleared

CRP (II) Calibrators

K030546510(k) TraditionalCleared Jun 2, 2003102-day reviewClass II21 CFR 862.1150

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

Denka Seiken Co., Ltd. · JIS Calibrator, Primary

Cleared on Jun 2, 2003 after a 102-day review. The FDA summary names its predicate without a number. 2 later devices descend from it.

Decided
Jun 2, 2003
Review
102 days
Class
Class II
Product code
JIS
Recalls
None
Predicates
0

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

Descendants, by year cleared 2005: 1 descendant cleared2019: 1 descendant cleared200020052010201520202025
  1. This deviceK030546 CRP (II) CalibratorsDenka Seiken Co., Ltd. · 2003
  2. Descendant · cites it directly · 1 of its ownK050836 CRP Diagnostic AssaySentinel Ch. Srl · 2005
  3. Descendant · 2 generations on · 0 of its ownK192118 CRP VarioSENTINEL CH. SpA · 2019

Most influential descendants

Showing 2 of 2 · See all
  • K050836CRP Diagnostic AssaySentinel Ch. Srl · 2005 · cites it directly1descendant
  • K192118CRP VarioSENTINEL CH. SpA · 2019 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K030546CRP (II) CalibratorsDenka Seiken Co., Ltd.2003—
+1K050836CRP Diagnostic AssaySentinel Ch. Srl2005—
+2K192118CRP VarioSENTINEL CH. SpA2019—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
201910
FIG. 1 — Lineage of K030546, 2003–2019Source: 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 JIS? 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
*—N High Sensitivity CRP Assay
Named without a submission number
—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K050836CRP Diagnostic AssaySentinel Ch. Srl20051

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, K050836 (Sentinel Ch. Srl, 2005) has gone furthest, with 1 descendant of its own.

How does its category compare?

All JIS devices

JIS Calibrator, Primary: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JIS

1in 2012

2012: 1
2007high 1 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JIS

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

Recalls per year · JIS

1in 2022

2008: 12011: 22012: 12016: 12018: 12020: 12021: 12022: 1
2007high 2 (2011) · low 0 (2007)2026

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

Adverse event reports per year · JIS

1in 2024

2010: 12011: 52012: 52013: 12015: 12016: 12017: 32018: 72019: 12020: 12022: 112024: 1
2007high 11 (2022) · low 0 (2007)2025

MAUDE reports naming product code JIS, 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—10
20090—00
20100—01
20110—25
20121—15
20130—01
20140—00
20150—01
20160—11
20170—03
20180—17
20190—01
20200—11
20210—10
20220—111
20230—00
20240—01
20250—00
20260—0—

What is it indicated for?

The CRP(II) Calibrators are intended to be used for the calibration of the CRP-Latex 0 x 2 SEIKEN Assay kit for quantitating CRP (C-reactive protein) in human serum and EDTA or lithium heparinized plasma samples.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K030546: CRP (II) Calibrators.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K030546

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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