510(k) Report

510(k) · Cleared

Cleared

R & D Systems Xeret Hematology Control

K100050510(k) SpecialCleared Jan 29, 201021-day reviewClass II21 CFR 864.8625

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

R&D Systems, Inc. · JPK Mixture, Hematology Quality Control

Cleared on Jan 29, 2010 as substantially equivalent to K042094 (R&D Systems, Inc., 2004) after a 21-day review. Its family tree reaches back 2 generations to 1991.

Decided
Jan 29, 2010
Review
21 days
Class
Class II
Product code
JPK
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K913879 (1991). No later device cites it as a predicate yet.

  1. Root · 2 generations backK913879 CBC-8K (TM) Hematology Control/MultipleR&D Systems, Inc. · 1991
  2. 1 generation backK042094 R&D CBC-XE Hematology ControlR&D Systems, Inc. · 2004
  3. This deviceK100050 R & D Systems Xeret Hematology ControlR&D Systems, Inc. · 2010
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K913879CBC-8K (TM) Hematology Control/MultipleR&D Systems, Inc.1991—
−1K042094R&D CBC-XE Hematology ControlR&D Systems, Inc.2004—
0 (this device)K100050R & D Systems Xeret Hematology ControlR&D Systems, Inc.2010—
FIG. 1 — Lineage of K100050, 1991–2010Source: 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.

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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
*K042094R&D CBC-XE Hematology Control
Summary page 1
…e Product Code: JPK Device Class: II Panel: Hematology (81) Predicate Device R&D Systems CBC-XE Hematology Control, (K042094) manufactured by R&D Systems, Inc. 614 McKinley Place N.E., Minneapolis, MN 55413. Description of Device The R&D Systems XERet H…
R&D Systems, Inc.2004—

Also cleared against K042094: 1 other device →

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 19 years and passes through 1 company; a new generation was cleared every 12.8 years on median.
  • None of the 2 ancestors has a recall.
  • 1 other device also cites its predicate K042094.

How does its category compare?

All JPK devices

JPK Mixture, Hematology Quality Control: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · JPK

4in 2016

2007: 52009: 52010: 42011: 12012: 22013: 12014: 22016: 4
2007high 5 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JPK

296in 2016

2007: 44 days median2009: 187 days median2010: 267 days median2016: 296 days median
2007high 296 (2016) · low 44 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · JPK

1in 2022

2007: 12010: 22011: 32012: 12020: 12021: 22022: 1
2007high 3 (2011) · low 0 (2008)2026

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

Adverse event reports per year · JPK

2in 2023

2007: 142008: 12010: 52011: 562012: 22014: 12019: 12020: 12021: 12023: 2
2007high 56 (2011) · low 0 (2009)2025

MAUDE reports naming product code JPK, 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
2007544114
20080—01
2009518700
2010426725
20111—356
20122—12
20131—00
20142—01
20150—00
2016429600
20170—00
20180—00
20190—01
20200—11
20210—21
20220—10
20230—02
20240—00
20250—00
20260—0—

What is it indicated for?

R&D XERet Control is a tni-level, assayed Hematology control designed to monitor values on Sysmexo hematology analyzers.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K100050: R & D Systems Xeret Hematology Control.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K100050

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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