510(k) Report

510(k) · Cleared

Recalled · Class II · 2018

Aia-Pack Tgab Assay

K981522510(k) TraditionalCleared Oct 8, 1998163-day reviewClass II21 CFR 866.5870Recalls 3

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

Tosoh Medics, Inc. · JZO System, Test, Thyroid Autoantibody

Cleared on Oct 8, 1998 after a 163-day review. FDA’s file for it is a 510(k) statement, which names no predicate. It has been recalled 3 times.

Decided
Oct 8, 1998
Review
163 days
Class
Class II
Product code
JZO
Recalls
3
Predicates
0

FDA’s file for it is a 510(k) statement, which names no predicate.

FIG. 1 — Lineage of K981522Source: FDA 510(k) database · 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 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JZO? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new JZO device

  1. #1 K250250 ADVIA Centaur Anti-Thyroid Peroxidase IIscore 10.5 · 2 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

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
Jun 5, 2018Class IIIZ-2827-2018Error in labelingDistribution of unapproved product labeling
Feb 8, 2017Class IIIZ-2169-2017Labeling mix-upsThe label contains two different methodologies. Quality Control values for non-FDA approved methodology (CL) are on the label in addition to the FDA approved methodology values (AIA). Two sets of instructions were included on the label.
Feb 23, 2012Class IIZ-1187-2021Nonconforming Material/ComponentSome combinations of Calibrator lots and AlA PACKS resulted in Calibrator #6 not giving a value, making the calibration unacceptable.

No ancestor or descendant has a Class I recall.

How does its category compare?

All JZO devices

JZO System, Test, Thyroid Autoantibody: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JZO

1in 2025

2008: 22009: 22010: 12016: 22020: 12023: 22024: 12025: 1
2007high 2 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JZO

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

Recalls per year · JZO

1in 2025

2025: 1
2007high 1 (2025) · low 0 (2007)2026

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

Adverse event reports per year · JZO

44in 2025

2010: 12011: 52012: 42013: 42014: 22015: 42016: 82017: 122018: 352019: 392020: 172021: 192022: 252023: 332024: 292025: 44
2007high 44 (2025) · low 0 (2007)2025

MAUDE reports naming product code JZO, 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
20082—00
20092—00
20101—01
20110—05
20120—04
20130—04
20140—02
20150—04
20162—08
20170—012
20180—035
20190—039
20201—017
20210—019
20220—025
20232—033
20241—029
20251—144
20260—0—

What is it indicated for?

AIA-PACK TgAb is intended for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of anti-thyroglobulin antibodies (TgAb) in human serum on specific TOSOH AIA System analyzers. Measurements obtained by this device aid in the diagnosis of autoimmune thyroid disorders, such as Graves’ disease and Hashimoto's disease.

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K981522: Aia-Pack Tgab Assay.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K981522

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026