510(k) Report

510(k) · Cleared

Recalled · Class II · 2019

Mission Trinity R (Level 1) (Level 2) (Level 3), (Level 1,2,3)

K093384510(k) TraditionalCleared Mar 10, 2010131-day reviewClass I21 CFR 862.1660Recalls 1

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

Diamond Diagnostics, Inc. · JJY Multi-Analyte Controls, All Kinds (Assayed)

Cleared on Mar 10, 2010 as substantially equivalent to K880447 (Bionostics, Inc., 1988) after a 131-day review. Its family tree reaches back 1 generation to 1988. It has been recalled once.

Decided
Mar 10, 2010
Review
131 days
Class
Class I
Product code
JJY
Recalls
1
Predicates
1

Its longest line of descent runs back 1 generation to K880447 (1988). No later device cites it as a predicate yet.

K880447 · Multi-Function Blood Gas Control · Bionostics, Inc. · 1988198519901995200020052010
K880447 · Multi-Function Blood Gas Control · Bionostics, Inc. · 19880
  1. Root · 1 generation backK880447 Multi-Function Blood Gas ControlBionostics, Inc. · 1988
  2. This deviceK093384 Mission Trinity R (Level 1) (Level 2) (Level 3), (Level 1,2,3)Diamond Diagnostics, Inc. · 2010
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K880447Multi-Function Blood Gas ControlBionostics, Inc.1988—
0 (this device)K093384Mission Trinity R (Level 1) (Level 2) (Level 3), (Level 1,2,3)Diamond Diagnostics, Inc.2010—
FIG. 1 — Lineage of K093384, 1988–2010Source: 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.

Planning a device in JJY? 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
*K880447Multi-Function Blood Gas Control
Summary page 2
…al RA 525 Blood Gas, Electrolyte, Metabolite, CO-OXimeter (Radiometer) Control Predicate 510(k) number(s): K880447 Comparison with predicate: Sim ilari…
Bionostics, Inc.1988—

Also cleared against K880447: 3 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)

Recalls of this device

DateClassRecallRoot causeReason
Feb 13, 2019Class IIZ-1057-2019Process controlAn error in the assignment of the control range pH in Blood Gas Control

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Its one ancestor has no recall.
  • 3 other devices also cite its predicate K880447.

How does its category compare?

All JJY devices

JJY Multi-Analyte Controls, All Kinds (Assayed): FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · JJY

3in 2017

2007: 112008: 72009: 82010: 102011: 142012: 132013: 162014: 102015: 42016: 12017: 3
2007high 16 (2013) · low 0 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JJY

78in 2017

2007: 49 days median2008: 54 days median2009: 80 days median2010: 109 days median2011: 120 days median2012: 40 days median2013: 82 days median2014: 49 days median2015: 153 days median2017: 78 days median
2007high 153 (2015) · low 40 (2012)2026

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

Recalls per year · JJY

2in 2025

2007: 52009: 22010: 62011: 12012: 32013: 22014: 22015: 12016: 32017: 42018: 32019: 42020: 62022: 32023: 32025: 22026 (partial year): 1
2007high 6 (2010) · low 0 (2008)2026

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

Adverse event reports per year · JJY

13in 2025

2007: 22008: 12009: 32010: 32011: 62012: 202013: 52014: 42015: 42016: 132017: 122018: 72019: 12020: 72021: 12023: 42024: 12025: 13
2007high 20 (2012) · low 0 (2022)2025

MAUDE reports naming product code JJY, 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
2007114952
200875401
200988023
20101010963
20111412016
20121340320
2013168225
2014104924
2015415314
20161—313
2017378412
20180—37
20190—41
20200—67
20210—01
20220—30
20230—34
20240—01
20250—213
20260—1—

What is it indicated for?

Mission Trinity R Control is intended to be used as an assayed quality control material for monitoring the precision and performance of the following analytes pH, pCO2, PO2, Na+, K, Ca+, Cl, glucose, and lactate on blood gas, electrolyte, and metabolite analyzers as well as tHb, %O2Hb, %O2Sat, %COHb, %MetHb, %O2Ct & %HHb on CO-Oximeter instrumentation.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K093384: Mission Trinity R (Level 1) (Level 2) (Level 3), (Level 1,2,3).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K093384

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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