510(k) Report

510(k) · Cleared

Cleared

Audit Microcv Protein Linearity Set

K101216510(k) TraditionalCleared Jan 14, 2011259-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

Aalto Scientific, Ltd. · JJY Multi-Analyte Controls, All Kinds (Assayed)

Cleared on Jan 14, 2011 as substantially equivalent to K042318 (Aalto Scientific, Ltd., 2004) after a 259-day review. Its family tree reaches back 3 generations to 1991. 2 later devices descend from it.

Decided
Jan 14, 2011
Review
259 days
Class
Class I
Product code
JJY
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K910440 (1991). 2 later devices descend from it, 2 citing it directly.

  1. Root · 3 generations backK910440 Document Reflectance II Linearity Test SetCasco Standards · 1991
  2. 2 generations backK023410 Validate Chem 10 Calibration Verification Test Set, Model 110Maine Standards Co. · 2003
  3. 1 generation backK042318 Audit Microcv General Chemistry Linearity SetAalto Scientific, Ltd. · 2004
  4. This deviceK101216 Audit Microcv Protein Linearity SetAalto Scientific, Ltd. · 2011
  5. Descendant · cites it directly · 0 of its ownK112742 Audit Microlq Spinal Fluid ControlAalto Scientific, Ltd. · 2012
  6. Descendant · cites it directly · 0 of its ownK112705 Audit (R) Microlq (TM) Serum Protein ControlAalto Scientific, Ltd. · 2012

Most influential descendants

Showing 2 of 2 · See all
  • K112742Audit Microlq Spinal Fluid ControlAalto Scientific, Ltd. · 2012 · cites it directly0descendants
  • K112705Audit (R) Microlq (TM) Serum Protein ControlAalto Scientific, Ltd. · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K910440Document Reflectance II Linearity Test SetCasco Standards1991—
−2K023410Validate Chem 10 Calibration Verification Test Set, Model 110Maine Standards Co.2003—
−1K042318Audit Microcv General Chemistry Linearity SetAalto Scientific, Ltd.2004—
0 (this device)K101216Audit Microcv Protein Linearity SetAalto Scientific, Ltd.2011—
+1K112742Audit Microlq Spinal Fluid ControlAalto Scientific, Ltd.2012—
+1K112705Audit (R) Microlq (TM) Serum Protein ControlAalto Scientific, Ltd.2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201220
FIG. 1 — Lineage of K101216, 1991–2012Source: 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
*K042318Audit Microcv General Chemistry Linearity Set
Summary page 1
…JJY E. Device to Which Substantial E quivalence is Claimed AuditTM MicroCVTM General Chemistry Linearity Set Aalto Scientific, Ltd., Carlsbad, CA K042318 F. Description of the Device The AuditTM MicroCVTM Protein Linearity Set is a hum…
Aalto Scientific, Ltd.2004—

Also cleared against K042318: 11 other devices →

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K112742Audit Microlq Spinal Fluid ControlAalto Scientific, Ltd.20120
K112705Audit (R) Microlq (TM) Serum Protein ControlAalto Scientific, Ltd.20120

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 20 years and passes through 3 companies; a new generation was cleared every 6.1 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K112742 (Aalto Scientific, Ltd., 2012) has gone furthest, with 0 descendants of its own.
  • 11 other devices also cite its predicate K042318.

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. 2011, 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?

The AuditTM MicroCVTM Protein Linearity is assayed quality control material consisting of five levels protein (human) based serum. Each level contains Alpha-lI-Antitrypsin, Complement C3, Complement C4, Immunoglobulin G, Immunoglobulin A, Immunoglobulin M and Transferrin analytes. The five levels demonstrate a linear relationship to each other for Alpha-1I-Antitrypsin, Complement C3, Complement C4, Immunoglobulin G, Immunoglobulin A, Immunoglobulin M…

Read the full statement (124 words)

The AuditTM MicroCVTM Protein Linearity is assayed quality control material consisting of five levels protein (human) based serum. Each level contains Alpha-lI-Antitrypsin, Complement C3, Complement C4, Immunoglobulin G, Immunoglobulin A, Immunoglobulin M and Transferrin analytes. The five levels demonstrate a linear relationship to each other for Alpha-1I-Antitrypsin, Complement C3, Complement C4, Immunoglobulin G, Immunoglobulin A, Immunoglobulin M, and Transferrin analytes. It is intended to simulate human patient serum samples and to detect systematic analytical deviations of laboratory testing procedures for Alpha-l -Antitrypsin, Complement C3, Complement C4, Immunoglobulin G, Immunoglobulin A, Immunoglobulin M, and Transferrin. The product is intended for use with quantitative assays on the indicated analyzer provided in the labeling. The Audit MicroCV Protein Linearity Set is "For In Vitro Diagnostic Use Only."

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K101216: Audit Microcv Protein Linearity Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K101216

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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