510(k) Report

510(k) · Cleared

Cleared

Precicontrol Clinchem Multi 1 and 2

K102016510(k) TraditionalCleared Sep 1, 201044-day reviewClass I21 CFR 862.1660

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

Roche Diagnostics · JJY Multi-Analyte Controls, All Kinds (Assayed)

Cleared on Sep 1, 2010 as substantially equivalent to K042389 (Roche Diagnostics Corp., 2004) after a 44-day review. Its family tree reaches back 3 generations to 1981. 1 later device descends from it.

Decided
Sep 1, 2010
Review
44 days
Class
Class I
Product code
JJY
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K811832 (1981). 1 later device descends from it, 1 citing it directly.

  1. Root · 3 generations backK811832 Precinorm U & Precipath U Human SerumBoehringer Mannheim Corp. · 1981
  2. 2 generations backK993360 Precinorm Universal Plus and Precipath Universal Plus Control SeraRoche Diagnostics Corp. · 1999
  3. 1 generation backK042389 Modification to Precinorm Universal Plus and Precipath Universal…Roche Diagnostics Corp. · 2004
  4. This deviceK102016 Precicontrol Clinchem Multi 1 and 2Roche Diagnostics · 2010
  5. Descendant · cites it directly · 0 of its ownK133330 C.F.a.S. Proteins, C.F.a.S. Pac, Precicontrol Clinchem Multi 1 & 2…Roche Diagnostics · 2013

Most influential descendants

Showing 1 of 1 · See all
  • K133330C.F.a.S. Proteins, C.F.a.S. Pac, Precicontrol Clinchem Multi 1 & 2, Precinorm Protein &…Roche Diagnostics · 2013 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K811832Precinorm U & Precipath U Human SerumBoehringer Mannheim Corp.1981—
−2K993360Precinorm Universal Plus and Precipath Universal Plus Control SeraRoche Diagnostics Corp.1999—
−1K042389Modification to Precinorm Universal Plus and Precipath Universal Plus Control…Roche Diagnostics Corp.2004—
0 (this device)K102016Precicontrol Clinchem Multi 1 and 2Roche Diagnostics2010—
+1K133330C.F.a.S. Proteins, C.F.a.S. Pac, Precicontrol Clinchem Multi 1 & 2, Precinorm…Roche Diagnostics2013—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
FIG. 1 — Lineage of K102016, 1981–2013Source: 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
*K042389Modification to Precinorm Universal Plus and Precipath Universal Plus Control Sera
Summary page 2
…in the value sheets. Predicate Roche claims substantial equivalence to the Roche Diagnostics Device Precinorm Universal Plus and Precipath Universal Plus (K042389). Continued on next page…
Roche Diagnostics Corp.2004—

Also cleared against K042389: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K133330C.F.a.S. Proteins, C.F.a.S. Pac, Precicontrol Clinchem Multi 1 & 2, Precinorm Protein &…Roche Diagnostics20130

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 29 years and passes through 3 companies; a new generation was cleared every 6.0 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K133330 (Roche Diagnostics, 2013) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K042389.

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?

PreciControl clinChem Multi 1 and 2 are for use in quality

control by monitoring accuracy and precision for the guantitative

methods as specified in the value sheets.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K102016: Precicontrol Clinchem Multi 1 and 2.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K102016

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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